Name: rs35967600
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs35967600

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:113981317-113981343 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₁₆ / del(T)₁₅ / del(T)₁₄ / d…
del(T)₁₆ / del(T)₁₅ / del(T)₁₄ / del(T)₁₃ / del(T)₁₂ / del(T)₁₁ / del(T)₁₀ / del(T)₉ / del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / insTTC(T)₄₁ / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₀ / dup(T)₁₁ / dup(T)₁₂ / ins(T)₁₂CC(T)₂₈ / dup(T)₁₃ / dup(T)₁₄ / ins(T)₁₄C(T)₂₇ / dup(T)₁₅ / dup(T)₁₆ / dup(T)₁₇ / dup(T)₁₈ / dup(T)₁₉ / dup(T)₂₀ / dup(T)₂₁ / dup(T)₂₂ / dup(T)₂₃ / dup(T)₂₄ / dup(T)₂₅ / dup(T)₂₆ / dup(T)₂₇ / ins(T)₂₈ / ins(T)₃₂ / ins(T)₃₄
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.01676 (204/12174, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LINC01191 : Intron Variant
LINC02992 : 2KB Upstream Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	12174	TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.96690	TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00041, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00706, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.01676, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00772, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00025, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00041, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00049, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.972091	0.004905	0.023004	32
European	Sub	10552	TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.96238	TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00815, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.01924, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00891, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00028, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00047, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00057, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.967881	0.00568	0.026439	32
African	Sub	1002	TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.9960	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0040, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	42	TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.98	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.02, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	960	TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.997	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.003, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	36	TTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	28	TTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	8	TTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	60	TTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	262	TTTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	46	TTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	216	TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.991	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.005, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.005, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	0.990654	0.0	0.009346	0

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	12174	(T)₂₇=0.96690	del(T)₁₆=0.00000, del(T)₁₅=0.00000, del(T)₁₄=0.00000, del(T)₁₃=0.00000, del(T)₁₂=0.00000, del(T)₁₁=0.00041, del(T)₁₀=0.00000, del(T)₉=0.00000, del(T)₈=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00706, dupT=0.01676, dupTT=0.00772, dupTTT=0.00000, dup(T)₄=0.00000, dup(T)₅=0.00000, dup(T)₆=0.00000, dup(T)₇=0.00000, dup(T)₈=0.00000, dup(T)₁₃=0.00025, dup(T)₁₄=0.00041, dup(T)₂₀=0.00049
Allele Frequency Aggregator	European	Sub	10552	(T)₂₇=0.96238	del(T)₁₆=0.00000, del(T)₁₅=0.00000, del(T)₁₄=0.00000, del(T)₁₃=0.00000, del(T)₁₂=0.00000, del(T)₁₁=0.00000, del(T)₁₀=0.00000, del(T)₉=0.00000, del(T)₈=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00815, dupT=0.01924, dupTT=0.00891, dupTTT=0.00000, dup(T)₄=0.00000, dup(T)₅=0.00000, dup(T)₆=0.00000, dup(T)₇=0.00000, dup(T)₈=0.00000, dup(T)₁₃=0.00028, dup(T)₁₄=0.00047, dup(T)₂₀=0.00057
Allele Frequency Aggregator	African	Sub	1002	(T)₂₇=0.9960	del(T)₁₆=0.0000, del(T)₁₅=0.0000, del(T)₁₄=0.0000, del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₁=0.0040, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0000, dup(T)₆=0.0000, dup(T)₇=0.0000, dup(T)₈=0.0000, dup(T)₁₃=0.0000, dup(T)₁₄=0.0000, dup(T)₂₀=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	262	(T)₂₇=1.000	del(T)₁₆=0.000, del(T)₁₅=0.000, del(T)₁₄=0.000, del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000, dup(T)₈=0.000, dup(T)₁₃=0.000, dup(T)₁₄=0.000, dup(T)₂₀=0.000
Allele Frequency Aggregator	Other	Sub	216	(T)₂₇=0.991	del(T)₁₆=0.000, del(T)₁₅=0.000, del(T)₁₄=0.000, del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.005, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.005, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000, dup(T)₈=0.000, dup(T)₁₃=0.000, dup(T)₁₄=0.000, dup(T)₂₀=0.000
Allele Frequency Aggregator	Latin American 1	Sub	60	(T)₂₇=1.00	del(T)₁₆=0.00, del(T)₁₅=0.00, del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00, dup(T)₁₃=0.00, dup(T)₁₄=0.00, dup(T)₂₀=0.00
Allele Frequency Aggregator	South Asian	Sub	46	(T)₂₇=1.00	del(T)₁₆=0.00, del(T)₁₅=0.00, del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00, dup(T)₁₃=0.00, dup(T)₁₄=0.00, dup(T)₂₀=0.00
Allele Frequency Aggregator	Asian	Sub	36	(T)₂₇=1.00	del(T)₁₆=0.00, del(T)₁₅=0.00, del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00, dup(T)₁₃=0.00, dup(T)₁₄=0.00, dup(T)₂₀=0.00

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 2	NC_000002.12:g.113981328_113981343del
GRCh38.p14 chr 2	NC_000002.12:g.113981329_113981343del
GRCh38.p14 chr 2	NC_000002.12:g.113981330_113981343del
GRCh38.p14 chr 2	NC_000002.12:g.113981331_113981343del
GRCh38.p14 chr 2	NC_000002.12:g.113981332_113981343del
GRCh38.p14 chr 2	NC_000002.12:g.113981333_113981343del
GRCh38.p14 chr 2	NC_000002.12:g.113981334_113981343del
GRCh38.p14 chr 2	NC_000002.12:g.113981335_113981343del
GRCh38.p14 chr 2	NC_000002.12:g.113981336_113981343del
GRCh38.p14 chr 2	NC_000002.12:g.113981337_113981343del
GRCh38.p14 chr 2	NC_000002.12:g.113981338_113981343del
GRCh38.p14 chr 2	NC_000002.12:g.113981339_113981343del
GRCh38.p14 chr 2	NC_000002.12:g.113981340_113981343del
GRCh38.p14 chr 2	NC_000002.12:g.113981341_113981343del
GRCh38.p14 chr 2	NC_000002.12:g.113981342_113981343del
GRCh38.p14 chr 2	NC_000002.12:g.113981343del
GRCh38.p14 chr 2	NC_000002.12:g.113981343dup
GRCh38.p14 chr 2	NC_000002.12:g.113981342_113981343dup
GRCh38.p14 chr 2	NC_000002.12:g.113981317_113981343T[29]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 2	NC_000002.12:g.113981341_113981343dup
GRCh38.p14 chr 2	NC_000002.12:g.113981340_113981343dup
GRCh38.p14 chr 2	NC_000002.12:g.113981339_113981343dup
GRCh38.p14 chr 2	NC_000002.12:g.113981338_113981343dup
GRCh38.p14 chr 2	NC_000002.12:g.113981337_113981343dup
GRCh38.p14 chr 2	NC_000002.12:g.113981336_113981343dup
GRCh38.p14 chr 2	NC_000002.12:g.113981335_113981343dup
GRCh38.p14 chr 2	NC_000002.12:g.113981334_113981343dup
GRCh38.p14 chr 2	NC_000002.12:g.113981333_113981343dup
GRCh38.p14 chr 2	NC_000002.12:g.113981332_113981343dup
GRCh38.p14 chr 2	NC_000002.12:g.113981317_113981343T[39]CCTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 2	NC_000002.12:g.113981331_113981343dup
GRCh38.p14 chr 2	NC_000002.12:g.113981330_113981343dup
GRCh38.p14 chr 2	NC_000002.12:g.113981317_113981343T[41]CTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 2	NC_000002.12:g.113981329_113981343dup
GRCh38.p14 chr 2	NC_000002.12:g.113981328_113981343dup
GRCh38.p14 chr 2	NC_000002.12:g.113981327_113981343dup
GRCh38.p14 chr 2	NC_000002.12:g.113981326_113981343dup
GRCh38.p14 chr 2	NC_000002.12:g.113981325_113981343dup
GRCh38.p14 chr 2	NC_000002.12:g.113981324_113981343dup
GRCh38.p14 chr 2	NC_000002.12:g.113981323_113981343dup
GRCh38.p14 chr 2	NC_000002.12:g.113981322_113981343dup
GRCh38.p14 chr 2	NC_000002.12:g.113981321_113981343dup
GRCh38.p14 chr 2	NC_000002.12:g.113981320_113981343dup
GRCh38.p14 chr 2	NC_000002.12:g.113981319_113981343dup
GRCh38.p14 chr 2	NC_000002.12:g.113981318_113981343dup
GRCh38.p14 chr 2	NC_000002.12:g.113981317_113981343dup
GRCh38.p14 chr 2	NC_000002.12:g.113981343_113981344insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 2	NC_000002.12:g.113981343_113981344insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 2	NC_000002.12:g.113981343_113981344insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 2	NC_000002.11:g.114738905_114738920del
GRCh37.p13 chr 2	NC_000002.11:g.114738906_114738920del
GRCh37.p13 chr 2	NC_000002.11:g.114738907_114738920del
GRCh37.p13 chr 2	NC_000002.11:g.114738908_114738920del
GRCh37.p13 chr 2	NC_000002.11:g.114738909_114738920del
GRCh37.p13 chr 2	NC_000002.11:g.114738910_114738920del
GRCh37.p13 chr 2	NC_000002.11:g.114738911_114738920del
GRCh37.p13 chr 2	NC_000002.11:g.114738912_114738920del
GRCh37.p13 chr 2	NC_000002.11:g.114738913_114738920del
GRCh37.p13 chr 2	NC_000002.11:g.114738914_114738920del
GRCh37.p13 chr 2	NC_000002.11:g.114738915_114738920del
GRCh37.p13 chr 2	NC_000002.11:g.114738916_114738920del
GRCh37.p13 chr 2	NC_000002.11:g.114738917_114738920del
GRCh37.p13 chr 2	NC_000002.11:g.114738918_114738920del
GRCh37.p13 chr 2	NC_000002.11:g.114738919_114738920del
GRCh37.p13 chr 2	NC_000002.11:g.114738920del
GRCh37.p13 chr 2	NC_000002.11:g.114738920dup
GRCh37.p13 chr 2	NC_000002.11:g.114738919_114738920dup
GRCh37.p13 chr 2	NC_000002.11:g.114738894_114738920T[29]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 2	NC_000002.11:g.114738918_114738920dup
GRCh37.p13 chr 2	NC_000002.11:g.114738917_114738920dup
GRCh37.p13 chr 2	NC_000002.11:g.114738916_114738920dup
GRCh37.p13 chr 2	NC_000002.11:g.114738915_114738920dup
GRCh37.p13 chr 2	NC_000002.11:g.114738914_114738920dup
GRCh37.p13 chr 2	NC_000002.11:g.114738913_114738920dup
GRCh37.p13 chr 2	NC_000002.11:g.114738912_114738920dup
GRCh37.p13 chr 2	NC_000002.11:g.114738911_114738920dup
GRCh37.p13 chr 2	NC_000002.11:g.114738910_114738920dup
GRCh37.p13 chr 2	NC_000002.11:g.114738909_114738920dup
GRCh37.p13 chr 2	NC_000002.11:g.114738894_114738920T[39]CCTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 2	NC_000002.11:g.114738908_114738920dup
GRCh37.p13 chr 2	NC_000002.11:g.114738907_114738920dup
GRCh37.p13 chr 2	NC_000002.11:g.114738894_114738920T[41]CTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 2	NC_000002.11:g.114738906_114738920dup
GRCh37.p13 chr 2	NC_000002.11:g.114738905_114738920dup
GRCh37.p13 chr 2	NC_000002.11:g.114738904_114738920dup
GRCh37.p13 chr 2	NC_000002.11:g.114738903_114738920dup
GRCh37.p13 chr 2	NC_000002.11:g.114738902_114738920dup
GRCh37.p13 chr 2	NC_000002.11:g.114738901_114738920dup
GRCh37.p13 chr 2	NC_000002.11:g.114738900_114738920dup
GRCh37.p13 chr 2	NC_000002.11:g.114738899_114738920dup
GRCh37.p13 chr 2	NC_000002.11:g.114738898_114738920dup
GRCh37.p13 chr 2	NC_000002.11:g.114738897_114738920dup
GRCh37.p13 chr 2	NC_000002.11:g.114738896_114738920dup
GRCh37.p13 chr 2	NC_000002.11:g.114738895_114738920dup
GRCh37.p13 chr 2	NC_000002.11:g.114738894_114738920dup
GRCh37.p13 chr 2	NC_000002.11:g.114738920_114738921insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 2	NC_000002.11:g.114738920_114738921insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 2	NC_000002.11:g.114738920_114738921insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: LINC01191, long intergenic non-protein coding RNA 1191 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LINC01191 transcript variant 1	NR_034128.1:n.	N/A	Intron Variant
LINC01191 transcript variant 2	NR_148507.1:n.	N/A	Intron Variant
LINC01191 transcript variant 3	NR_148508.1:n.	N/A	Intron Variant
LINC01191 transcript variant 4	NR_148509.1:n.	N/A	Intron Variant

Gene: LINC02992, long intergenic non-protein coding RNA 2992 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
LINC02992 transcript	NR_034130.1:n.	N/A	Upstream Transcript Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(T)₂₇=	del(T)₁₆	del(T)₁₅	del(T)₁₄	del(T)₁₃	del(T)₁₂	del(T)₁₁	del(T)₁₀	del(T)₉	del(T)₈	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	insTTC(T)₄₁	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₀	dup(T)₁₁	dup(T)₁₂	ins(T)₁₂CC(T)₂₈	dup(T)₁₃	dup(T)₁₄	ins(T)₁₄C(T)₂₇	dup(T)₁₅	dup(T)₁₆	dup(T)₁₇	dup(T)₁₈	dup(T)₁₉	dup(T)₂₀	dup(T)₂₁	dup(T)₂₂	dup(T)₂₃	dup(T)₂₄	dup(T)₂₅	dup(T)₂₆	dup(T)₂₇	ins(T)₂₈	ins(T)₃₂	ins(T)₃₄
GRCh38.p14 chr 2	NC_000002.12:g.113981317_113981343=	NC_000002.12:g.113981328_113981343del	NC_000002.12:g.113981329_113981343del	NC_000002.12:g.113981330_113981343del	NC_000002.12:g.113981331_113981343del	NC_000002.12:g.113981332_113981343del	NC_000002.12:g.113981333_113981343del	NC_000002.12:g.113981334_113981343del	NC_000002.12:g.113981335_113981343del	NC_000002.12:g.113981336_113981343del	NC_000002.12:g.113981337_113981343del	NC_000002.12:g.113981338_113981343del	NC_000002.12:g.113981339_113981343del	NC_000002.12:g.113981340_113981343del	NC_000002.12:g.113981341_113981343del	NC_000002.12:g.113981342_113981343del	NC_000002.12:g.113981343del	NC_000002.12:g.113981343dup	NC_000002.12:g.113981342_113981343dup	NC_000002.12:g.113981317_113981343T[29]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000002.12:g.113981341_113981343dup	NC_000002.12:g.113981340_113981343dup	NC_000002.12:g.113981339_113981343dup	NC_000002.12:g.113981338_113981343dup	NC_000002.12:g.113981337_113981343dup	NC_000002.12:g.113981336_113981343dup	NC_000002.12:g.113981335_113981343dup	NC_000002.12:g.113981334_113981343dup	NC_000002.12:g.113981333_113981343dup	NC_000002.12:g.113981332_113981343dup	NC_000002.12:g.113981317_113981343T[39]CCTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000002.12:g.113981331_113981343dup	NC_000002.12:g.113981330_113981343dup	NC_000002.12:g.113981317_113981343T[41]CTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000002.12:g.113981329_113981343dup	NC_000002.12:g.113981328_113981343dup	NC_000002.12:g.113981327_113981343dup	NC_000002.12:g.113981326_113981343dup	NC_000002.12:g.113981325_113981343dup	NC_000002.12:g.113981324_113981343dup	NC_000002.12:g.113981323_113981343dup	NC_000002.12:g.113981322_113981343dup	NC_000002.12:g.113981321_113981343dup	NC_000002.12:g.113981320_113981343dup	NC_000002.12:g.113981319_113981343dup	NC_000002.12:g.113981318_113981343dup	NC_000002.12:g.113981317_113981343dup	NC_000002.12:g.113981343_113981344insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:g.113981343_113981344insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:g.113981343_113981344insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 2	NC_000002.11:g.114738894_114738920=	NC_000002.11:g.114738905_114738920del	NC_000002.11:g.114738906_114738920del	NC_000002.11:g.114738907_114738920del	NC_000002.11:g.114738908_114738920del	NC_000002.11:g.114738909_114738920del	NC_000002.11:g.114738910_114738920del	NC_000002.11:g.114738911_114738920del	NC_000002.11:g.114738912_114738920del	NC_000002.11:g.114738913_114738920del	NC_000002.11:g.114738914_114738920del	NC_000002.11:g.114738915_114738920del	NC_000002.11:g.114738916_114738920del	NC_000002.11:g.114738917_114738920del	NC_000002.11:g.114738918_114738920del	NC_000002.11:g.114738919_114738920del	NC_000002.11:g.114738920del	NC_000002.11:g.114738920dup	NC_000002.11:g.114738919_114738920dup	NC_000002.11:g.114738894_114738920T[29]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000002.11:g.114738918_114738920dup	NC_000002.11:g.114738917_114738920dup	NC_000002.11:g.114738916_114738920dup	NC_000002.11:g.114738915_114738920dup	NC_000002.11:g.114738914_114738920dup	NC_000002.11:g.114738913_114738920dup	NC_000002.11:g.114738912_114738920dup	NC_000002.11:g.114738911_114738920dup	NC_000002.11:g.114738910_114738920dup	NC_000002.11:g.114738909_114738920dup	NC_000002.11:g.114738894_114738920T[39]CCTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000002.11:g.114738908_114738920dup	NC_000002.11:g.114738907_114738920dup	NC_000002.11:g.114738894_114738920T[41]CTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000002.11:g.114738906_114738920dup	NC_000002.11:g.114738905_114738920dup	NC_000002.11:g.114738904_114738920dup	NC_000002.11:g.114738903_114738920dup	NC_000002.11:g.114738902_114738920dup	NC_000002.11:g.114738901_114738920dup	NC_000002.11:g.114738900_114738920dup	NC_000002.11:g.114738899_114738920dup	NC_000002.11:g.114738898_114738920dup	NC_000002.11:g.114738897_114738920dup	NC_000002.11:g.114738896_114738920dup	NC_000002.11:g.114738895_114738920dup	NC_000002.11:g.114738894_114738920dup	NC_000002.11:g.114738920_114738921insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.11:g.114738920_114738921insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.11:g.114738920_114738921insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

73 SubSNP, 61 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80503237	Dec 15, 2007 (138)
2	HGSV	ss81525617	Dec 15, 2007 (130)
3	HUMANGENOME_JCVI	ss95963786	Mar 15, 2016 (147)
4	PJP	ss294998206	May 09, 2011 (137)
5	SWEGEN	ss2990212831	Nov 08, 2017 (151)
6	MCHAISSO	ss3065760210	Nov 17, 2017 (151)
7	EVA	ss3827160364	Apr 25, 2020 (154)
8	GNOMAD	ss4048619340	Apr 26, 2021 (155)
9	GNOMAD	ss4048619358	Apr 26, 2021 (155)
10	GNOMAD	ss4048619360	Apr 26, 2021 (155)
11	GNOMAD	ss4048619362	Apr 26, 2021 (155)
12	GNOMAD	ss4048619363	Apr 26, 2021 (155)
13	GNOMAD	ss4048619364	Apr 26, 2021 (155)
14	GNOMAD	ss4048619365	Apr 26, 2021 (155)
15	GNOMAD	ss4048619366	Apr 26, 2021 (155)
16	GNOMAD	ss4048619367	Apr 26, 2021 (155)
17	GNOMAD	ss4048619368	Apr 26, 2021 (155)
18	GNOMAD	ss4048619371	Apr 26, 2021 (155)
19	GNOMAD	ss4048619372	Apr 26, 2021 (155)
20	GNOMAD	ss4048619374	Apr 26, 2021 (155)
21	GNOMAD	ss4048619375	Apr 26, 2021 (155)
22	GNOMAD	ss4048619377	Apr 26, 2021 (155)
23	GNOMAD	ss4048619379	Apr 26, 2021 (155)
24	GNOMAD	ss4048619380	Apr 26, 2021 (155)
25	GNOMAD	ss4048619381	Apr 26, 2021 (155)
26	GNOMAD	ss4048619382	Apr 26, 2021 (155)
27	GNOMAD	ss4048619383	Apr 26, 2021 (155)
28	GNOMAD	ss4048619384	Apr 26, 2021 (155)
29	GNOMAD	ss4048619385	Apr 26, 2021 (155)
30	GNOMAD	ss4048619386	Apr 26, 2021 (155)
31	GNOMAD	ss4048619387	Apr 26, 2021 (155)
32	GNOMAD	ss4048619388	Apr 26, 2021 (155)
33	GNOMAD	ss4048619389	Apr 26, 2021 (155)
34	GNOMAD	ss4048619391	Apr 26, 2021 (155)
35	GNOMAD	ss4048619392	Apr 26, 2021 (155)
36	GNOMAD	ss4048619393	Apr 26, 2021 (155)
37	GNOMAD	ss4048619394	Apr 26, 2021 (155)
38	GNOMAD	ss4048619395	Apr 26, 2021 (155)
39	GNOMAD	ss4048619396	Apr 26, 2021 (155)
40	GNOMAD	ss4048619397	Apr 26, 2021 (155)
41	GNOMAD	ss4048619398	Apr 26, 2021 (155)
42	GNOMAD	ss4048619399	Apr 26, 2021 (155)
43	GNOMAD	ss4048619400	Apr 26, 2021 (155)
44	GNOMAD	ss4048619401	Apr 26, 2021 (155)
45	GNOMAD	ss4048619402	Apr 26, 2021 (155)
46	GNOMAD	ss4048619403	Apr 26, 2021 (155)
47	GNOMAD	ss4048619404	Apr 26, 2021 (155)
48	GNOMAD	ss4048619405	Apr 26, 2021 (155)
49	GNOMAD	ss4048619406	Apr 26, 2021 (155)
50	GNOMAD	ss4048619407	Apr 26, 2021 (155)
51	GNOMAD	ss4048619408	Apr 26, 2021 (155)
52	GNOMAD	ss4048619409	Apr 26, 2021 (155)
53	GNOMAD	ss4048619410	Apr 26, 2021 (155)
54	GNOMAD	ss4048619411	Apr 26, 2021 (155)
55	GNOMAD	ss4048619412	Apr 26, 2021 (155)
56	GNOMAD	ss4048619413	Apr 26, 2021 (155)
57	TOMMO_GENOMICS	ss5153295581	Apr 26, 2021 (155)
58	TOMMO_GENOMICS	ss5153295582	Apr 26, 2021 (155)
59	TOMMO_GENOMICS	ss5153295583	Apr 26, 2021 (155)
60	TOMMO_GENOMICS	ss5153295584	Apr 26, 2021 (155)
61	TOMMO_GENOMICS	ss5153295585	Apr 26, 2021 (155)
62	TOMMO_GENOMICS	ss5153295586	Apr 26, 2021 (155)
63	1000G_HIGH_COVERAGE	ss5249567501	Oct 12, 2022 (156)
64	1000G_HIGH_COVERAGE	ss5249567502	Oct 12, 2022 (156)
65	HUGCELL_USP	ss5449451797	Oct 12, 2022 (156)
66	HUGCELL_USP	ss5449451798	Oct 12, 2022 (156)
67	TOMMO_GENOMICS	ss5683250477	Oct 12, 2022 (156)
68	TOMMO_GENOMICS	ss5683250478	Oct 12, 2022 (156)
69	TOMMO_GENOMICS	ss5683250479	Oct 12, 2022 (156)
70	TOMMO_GENOMICS	ss5683250480	Oct 12, 2022 (156)
71	TOMMO_GENOMICS	ss5683250482	Oct 12, 2022 (156)
72	EVA	ss5820632236	Oct 12, 2022 (156)
73	EVA	ss5931886351	Oct 12, 2022 (156)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
94	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
95	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
96	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
97	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
98	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
99	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
100	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
101	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
102	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
103	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
104	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
105	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
106	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
107	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
108	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
109	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
110	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
111	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
112	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
113	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
114	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
115	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
116	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
117	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
118	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
119	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
120	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
121	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
122	gnomAD - Genomes Submission ignored due to conflicting rows: Row 70175044 (NC_000002.12:113981316::T 6469/44160) Row 70175062 (NC_000002.12:113981316::TT 1615/44042) Row 70175064 (NC_000002.12:113981316::TTT 971/44144)...	-	Apr 26, 2021 (155)
123	8.3KJPN Submission ignored due to conflicting rows: Row 11264888 (NC_000002.11:114738893::T 4648/16156) Row 11264889 (NC_000002.11:114738893:TTTTTTTTTT: 55/16156) Row 11264890 (NC_000002.11:114738893::TT 235/16156)...	-	Apr 26, 2021 (155)
124	8.3KJPN Submission ignored due to conflicting rows: Row 11264888 (NC_000002.11:114738893::T 4648/16156) Row 11264889 (NC_000002.11:114738893:TTTTTTTTTT: 55/16156) Row 11264890 (NC_000002.11:114738893::TT 235/16156)...	-	Apr 26, 2021 (155)
125	8.3KJPN Submission ignored due to conflicting rows: Row 11264888 (NC_000002.11:114738893::T 4648/16156) Row 11264889 (NC_000002.11:114738893:TTTTTTTTTT: 55/16156) Row 11264890 (NC_000002.11:114738893::TT 235/16156)...	-	Apr 26, 2021 (155)
126	8.3KJPN Submission ignored due to conflicting rows: Row 11264888 (NC_000002.11:114738893::T 4648/16156) Row 11264889 (NC_000002.11:114738893:TTTTTTTTTT: 55/16156) Row 11264890 (NC_000002.11:114738893::TT 235/16156)...	-	Apr 26, 2021 (155)
127	8.3KJPN Submission ignored due to conflicting rows: Row 11264888 (NC_000002.11:114738893::T 4648/16156) Row 11264889 (NC_000002.11:114738893:TTTTTTTTTT: 55/16156) Row 11264890 (NC_000002.11:114738893::TT 235/16156)...	-	Apr 26, 2021 (155)
128	8.3KJPN Submission ignored due to conflicting rows: Row 11264888 (NC_000002.11:114738893::T 4648/16156) Row 11264889 (NC_000002.11:114738893:TTTTTTTTTT: 55/16156) Row 11264890 (NC_000002.11:114738893::TT 235/16156)...	-	Apr 26, 2021 (155)
129	14KJPN Submission ignored due to conflicting rows: Row 17087581 (NC_000002.12:113981316::T 7336/22964) Row 17087582 (NC_000002.12:113981316::TT 351/22964) Row 17087583 (NC_000002.12:113981316:TTTTTTTTTT: 97/22964)...	-	Oct 12, 2022 (156)
130	14KJPN Submission ignored due to conflicting rows: Row 17087581 (NC_000002.12:113981316::T 7336/22964) Row 17087582 (NC_000002.12:113981316::TT 351/22964) Row 17087583 (NC_000002.12:113981316:TTTTTTTTTT: 97/22964)...	-	Oct 12, 2022 (156)
131	14KJPN Submission ignored due to conflicting rows: Row 17087581 (NC_000002.12:113981316::T 7336/22964) Row 17087582 (NC_000002.12:113981316::TT 351/22964) Row 17087583 (NC_000002.12:113981316:TTTTTTTTTT: 97/22964)...	-	Oct 12, 2022 (156)
132	14KJPN Submission ignored due to conflicting rows: Row 17087581 (NC_000002.12:113981316::T 7336/22964) Row 17087582 (NC_000002.12:113981316::TT 351/22964) Row 17087583 (NC_000002.12:113981316:TTTTTTTTTT: 97/22964)...	-	Oct 12, 2022 (156)
133	14KJPN Submission ignored due to conflicting rows: Row 17087581 (NC_000002.12:113981316::T 7336/22964) Row 17087582 (NC_000002.12:113981316::TT 351/22964) Row 17087583 (NC_000002.12:113981316:TTTTTTTTTT: 97/22964)...	-	Oct 12, 2022 (156)
134	ALFA	NC_000002.12 - 113981317	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs66840234	Feb 26, 2009 (130)
rs72063839	May 11, 2012 (137)
rs151011931	May 11, 2012 (137)
rs59062492	May 24, 2008 (130)
rs60457195	Apr 25, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4048619413	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTT:	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
9691397057	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4048619412	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTT:	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
9691397057	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4048619411	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTT:	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
9691397057	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4048619410	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTT:	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
9691397057	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4048619409	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTT:	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
9691397057	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4048619408, ss5249567501, ss5449451798, ss5931886351	NC_000002.12:113981316:TTTTTTTTTTT:	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
9691397057	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss5153295582	NC_000002.11:114738893:TTTTTTTTTT:	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4048619407, ss5683250479	NC_000002.12:113981316:TTTTTTTTTT:	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
9691397057	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4048619406	NC_000002.12:113981316:TTTTTTTTT:	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
9691397057	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4048619405	NC_000002.12:113981316:TTTTTTTT:	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
9691397057	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4048619404	NC_000002.12:113981316:TTTTTTT:	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
9691397057	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4048619403	NC_000002.12:113981316:TTTTTT:	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
9691397057	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619402	NC_000002.12:113981316:TTTTT:	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
9691397057	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619401	NC_000002.12:113981316:TTTT:	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
9691397057	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619400	NC_000002.12:113981316:TTT:	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
9691397057	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3065760210, ss4048619399	NC_000002.12:113981316:TT:	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9691397057	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss80503237	NC_000002.9:114455149:T:	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss2990212831, ss5153295584	NC_000002.11:114738893:T:	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619398, ss5449451797, ss5683250480	NC_000002.12:113981316:T:	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9691397057	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss81525617	NT_022135.16:4487582:T:	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss294998206	NC_000002.10:114455364::T	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5153295581	NC_000002.11:114738893::T	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619340, ss5683250477	NC_000002.12:113981316::T	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9691397057	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5153295583, ss5820632236	NC_000002.11:114738893::TT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619358, ss5683250478	NC_000002.12:113981316::TT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9691397057	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss95963786	NT_022135.16:4487583::TT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619393	NC_000002.12:113981316::TTTTTTTTTT… NC_000002.12:113981316::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3827160364, ss5153295585	NC_000002.11:114738893::TTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619360, ss5249567502	NC_000002.12:113981316::TTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9691397057	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619362	NC_000002.12:113981316::TTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9691397057	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619363	NC_000002.12:113981316::TTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9691397057	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619364	NC_000002.12:113981316::TTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9691397057	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619365	NC_000002.12:113981316::TTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9691397057	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619366	NC_000002.12:113981316::TTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9691397057	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619367	NC_000002.12:113981316::TTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619368	NC_000002.12:113981316::TTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619371	NC_000002.12:113981316::TTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619372	NC_000002.12:113981316::TTTTTTTTTT… NC_000002.12:113981316::TTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619396	NC_000002.12:113981316::TTTTTTTTTT… NC_000002.12:113981316::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCCT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCCTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619374, ss5683250482	NC_000002.12:113981316::TTTTTTTTTT… NC_000002.12:113981316::TTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9691397057	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619375	NC_000002.12:113981316::TTTTTTTTTT… NC_000002.12:113981316::TTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9691397057	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619397	NC_000002.12:113981316::TTTTTTTTTT… NC_000002.12:113981316::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTC	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5153295586	NC_000002.11:114738893::TTTTTTTTTT… NC_000002.11:114738893::TTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619377	NC_000002.12:113981316::TTTTTTTTTT… NC_000002.12:113981316::TTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619379	NC_000002.12:113981316::TTTTTTTTTT… NC_000002.12:113981316::TTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619380	NC_000002.12:113981316::TTTTTTTTTT… NC_000002.12:113981316::TTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619381	NC_000002.12:113981316::TTTTTTTTTT… NC_000002.12:113981316::TTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619382	NC_000002.12:113981316::TTTTTTTTTT… NC_000002.12:113981316::TTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619383	NC_000002.12:113981316::TTTTTTTTTT… NC_000002.12:113981316::TTTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9691397057	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619384	NC_000002.12:113981316::TTTTTTTTTT… NC_000002.12:113981316::TTTTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619385	NC_000002.12:113981316::TTTTTTTTTT… NC_000002.12:113981316::TTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619386	NC_000002.12:113981316::TTTTTTTTTT… NC_000002.12:113981316::TTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619387	NC_000002.12:113981316::TTTTTTTTTT… NC_000002.12:113981316::TTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619388	NC_000002.12:113981316::TTTTTTTTTT… NC_000002.12:113981316::TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619389	NC_000002.12:113981316::TTTTTTTTTT… NC_000002.12:113981316::TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619391	NC_000002.12:113981316::TTTTTTTTTT… NC_000002.12:113981316::TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619392	NC_000002.12:113981316::TTTTTTTTTT… NC_000002.12:113981316::TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619394	NC_000002.12:113981316::TTTTTTTTTT… NC_000002.12:113981316::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4048619395	NC_000002.12:113981316::TTTTTTTTTT… NC_000002.12:113981316::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:113981316:TTTTTTTTTTT… NC_000002.12:113981316:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs35967600

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs35967600