Name: rs71546560
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.

rs71546560

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:27693488-27693515 (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)₂₅ / del(T)₁₆ / del(T)₁₅ / d…
del(T)₂₅ / 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 / 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 / dup(T)₁₃ / dup(T)₁₅ / dup(T)₁₈ / dup(T)₂₁
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₁₀=0.01994 (222/11136, ALFA)
del(T)₁₀=0.4149 (2078/5008, 1000G)
dup(T)₆=0.009 (5/588, NorthernSweden) (+ 1 more)
(T)₂₈=0.00 (0/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LINC01012 : 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	11136	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.95618	TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.01994, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.01715, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00135, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00216, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00180, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00144, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.964206	0.00261	0.033184	32
European	Sub	9058	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.9461	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0245, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0211, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0017, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0026, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0022, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0018, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.955607	0.003237	0.041156	30
African	Sub	1246	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	36	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1210	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	48	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	44	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	4	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	82	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	388	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	44	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	270	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A

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	11136	(T)₂₈=0.95618	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=0.01994, 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=0.00180, dupT=0.01715, dupTT=0.00144, dupTTT=0.00216, dup(T)₄=0.00135, dup(T)₅=0.00000, dup(T)₉=0.00000
Allele Frequency Aggregator	European	Sub	9058	(T)₂₈=0.9461	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=0.0000, del(T)₁₀=0.0245, 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=0.0022, dupT=0.0211, dupTT=0.0018, dupTTT=0.0026, dup(T)₄=0.0017, dup(T)₅=0.0000, dup(T)₉=0.0000
Allele Frequency Aggregator	African	Sub	1246	(T)₂₈=1.0000	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=0.0000, 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)₉=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	388	(T)₂₈=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)₉=0.000
Allele Frequency Aggregator	Other	Sub	270	(T)₂₈=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)₉=0.000
Allele Frequency Aggregator	Latin American 1	Sub	82	(T)₂₈=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)₉=0.00
Allele Frequency Aggregator	Asian	Sub	48	(T)₂₈=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)₉=0.00
Allele Frequency Aggregator	South Asian	Sub	44	(T)₂₈=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)₉=0.00
1000Genomes	Global	Study-wide	5008	(T)₂₈=0.5851	del(T)₁₀=0.4149
1000Genomes	African	Sub	1322	(T)₂₈=0.5204	del(T)₁₀=0.4796
1000Genomes	East Asian	Sub	1008	(T)₂₈=0.6042	del(T)₁₀=0.3958
1000Genomes	Europe	Sub	1006	(T)₂₈=0.6491	del(T)₁₀=0.3509
1000Genomes	South Asian	Sub	978	(T)₂₈=0.567	del(T)₁₀=0.433
1000Genomes	American	Sub	694	(T)₂₈=0.612	del(T)₁₀=0.388
Northern Sweden	ACPOP	Study-wide	588	- No frequency provided	dup(T)₆=0.009
The Danish reference pan genome	Danish	Study-wide	40	(T)₂₈=0.00	del(T)₂₅=1.00

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 6	NC_000006.12:g.27693491_27693515del
GRCh38.p14 chr 6	NC_000006.12:g.27693500_27693515del
GRCh38.p14 chr 6	NC_000006.12:g.27693501_27693515del
GRCh38.p14 chr 6	NC_000006.12:g.27693502_27693515del
GRCh38.p14 chr 6	NC_000006.12:g.27693503_27693515del
GRCh38.p14 chr 6	NC_000006.12:g.27693504_27693515del
GRCh38.p14 chr 6	NC_000006.12:g.27693505_27693515del
GRCh38.p14 chr 6	NC_000006.12:g.27693506_27693515del
GRCh38.p14 chr 6	NC_000006.12:g.27693507_27693515del
GRCh38.p14 chr 6	NC_000006.12:g.27693508_27693515del
GRCh38.p14 chr 6	NC_000006.12:g.27693509_27693515del
GRCh38.p14 chr 6	NC_000006.12:g.27693510_27693515del
GRCh38.p14 chr 6	NC_000006.12:g.27693511_27693515del
GRCh38.p14 chr 6	NC_000006.12:g.27693512_27693515del
GRCh38.p14 chr 6	NC_000006.12:g.27693513_27693515del
GRCh38.p14 chr 6	NC_000006.12:g.27693514_27693515del
GRCh38.p14 chr 6	NC_000006.12:g.27693515del
GRCh38.p14 chr 6	NC_000006.12:g.27693515dup
GRCh38.p14 chr 6	NC_000006.12:g.27693514_27693515dup
GRCh38.p14 chr 6	NC_000006.12:g.27693513_27693515dup
GRCh38.p14 chr 6	NC_000006.12:g.27693512_27693515dup
GRCh38.p14 chr 6	NC_000006.12:g.27693511_27693515dup
GRCh38.p14 chr 6	NC_000006.12:g.27693510_27693515dup
GRCh38.p14 chr 6	NC_000006.12:g.27693509_27693515dup
GRCh38.p14 chr 6	NC_000006.12:g.27693508_27693515dup
GRCh38.p14 chr 6	NC_000006.12:g.27693507_27693515dup
GRCh38.p14 chr 6	NC_000006.12:g.27693506_27693515dup
GRCh38.p14 chr 6	NC_000006.12:g.27693505_27693515dup
GRCh38.p14 chr 6	NC_000006.12:g.27693504_27693515dup
GRCh38.p14 chr 6	NC_000006.12:g.27693503_27693515dup
GRCh38.p14 chr 6	NC_000006.12:g.27693501_27693515dup
GRCh38.p14 chr 6	NC_000006.12:g.27693498_27693515dup
GRCh38.p14 chr 6	NC_000006.12:g.27693495_27693515dup
GRCh37.p13 chr 6	NC_000006.11:g.27661270_27661294del
GRCh37.p13 chr 6	NC_000006.11:g.27661279_27661294del
GRCh37.p13 chr 6	NC_000006.11:g.27661280_27661294del
GRCh37.p13 chr 6	NC_000006.11:g.27661281_27661294del
GRCh37.p13 chr 6	NC_000006.11:g.27661282_27661294del
GRCh37.p13 chr 6	NC_000006.11:g.27661283_27661294del
GRCh37.p13 chr 6	NC_000006.11:g.27661284_27661294del
GRCh37.p13 chr 6	NC_000006.11:g.27661285_27661294del
GRCh37.p13 chr 6	NC_000006.11:g.27661286_27661294del
GRCh37.p13 chr 6	NC_000006.11:g.27661287_27661294del
GRCh37.p13 chr 6	NC_000006.11:g.27661288_27661294del
GRCh37.p13 chr 6	NC_000006.11:g.27661289_27661294del
GRCh37.p13 chr 6	NC_000006.11:g.27661290_27661294del
GRCh37.p13 chr 6	NC_000006.11:g.27661291_27661294del
GRCh37.p13 chr 6	NC_000006.11:g.27661292_27661294del
GRCh37.p13 chr 6	NC_000006.11:g.27661293_27661294del
GRCh37.p13 chr 6	NC_000006.11:g.27661294del
GRCh37.p13 chr 6	NC_000006.11:g.27661294dup
GRCh37.p13 chr 6	NC_000006.11:g.27661293_27661294dup
GRCh37.p13 chr 6	NC_000006.11:g.27661292_27661294dup
GRCh37.p13 chr 6	NC_000006.11:g.27661291_27661294dup
GRCh37.p13 chr 6	NC_000006.11:g.27661290_27661294dup
GRCh37.p13 chr 6	NC_000006.11:g.27661289_27661294dup
GRCh37.p13 chr 6	NC_000006.11:g.27661288_27661294dup
GRCh37.p13 chr 6	NC_000006.11:g.27661287_27661294dup
GRCh37.p13 chr 6	NC_000006.11:g.27661286_27661294dup
GRCh37.p13 chr 6	NC_000006.11:g.27661285_27661294dup
GRCh37.p13 chr 6	NC_000006.11:g.27661284_27661294dup
GRCh37.p13 chr 6	NC_000006.11:g.27661283_27661294dup
GRCh37.p13 chr 6	NC_000006.11:g.27661282_27661294dup
GRCh37.p13 chr 6	NC_000006.11:g.27661280_27661294dup
GRCh37.p13 chr 6	NC_000006.11:g.27661277_27661294dup
GRCh37.p13 chr 6	NC_000006.11:g.27661274_27661294dup

Gene: LINC01012, long intergenic non-protein coding RNA 1012 (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
LINC01012 transcript variant 1	NR_038292.1:n.	N/A	Upstream Transcript Variant
LINC01012 transcript variant 2	NR_038293.1:n.	N/A	Upstream Transcript Variant
LINC01012 transcript variant 3	NR_038294.1: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)₂₈=	del(T)₂₅	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	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	dup(T)₁₃	dup(T)₁₅	dup(T)₁₈	dup(T)₂₁
GRCh38.p14 chr 6	NC_000006.12:g.27693488_27693515=	NC_000006.12:g.27693491_27693515del	NC_000006.12:g.27693500_27693515del	NC_000006.12:g.27693501_27693515del	NC_000006.12:g.27693502_27693515del	NC_000006.12:g.27693503_27693515del	NC_000006.12:g.27693504_27693515del	NC_000006.12:g.27693505_27693515del	NC_000006.12:g.27693506_27693515del	NC_000006.12:g.27693507_27693515del	NC_000006.12:g.27693508_27693515del	NC_000006.12:g.27693509_27693515del	NC_000006.12:g.27693510_27693515del	NC_000006.12:g.27693511_27693515del	NC_000006.12:g.27693512_27693515del	NC_000006.12:g.27693513_27693515del	NC_000006.12:g.27693514_27693515del	NC_000006.12:g.27693515del	NC_000006.12:g.27693515dup	NC_000006.12:g.27693514_27693515dup	NC_000006.12:g.27693513_27693515dup	NC_000006.12:g.27693512_27693515dup	NC_000006.12:g.27693511_27693515dup	NC_000006.12:g.27693510_27693515dup	NC_000006.12:g.27693509_27693515dup	NC_000006.12:g.27693508_27693515dup	NC_000006.12:g.27693507_27693515dup	NC_000006.12:g.27693506_27693515dup	NC_000006.12:g.27693505_27693515dup	NC_000006.12:g.27693504_27693515dup	NC_000006.12:g.27693503_27693515dup	NC_000006.12:g.27693501_27693515dup	NC_000006.12:g.27693498_27693515dup	NC_000006.12:g.27693495_27693515dup
GRCh37.p13 chr 6	NC_000006.11:g.27661267_27661294=	NC_000006.11:g.27661270_27661294del	NC_000006.11:g.27661279_27661294del	NC_000006.11:g.27661280_27661294del	NC_000006.11:g.27661281_27661294del	NC_000006.11:g.27661282_27661294del	NC_000006.11:g.27661283_27661294del	NC_000006.11:g.27661284_27661294del	NC_000006.11:g.27661285_27661294del	NC_000006.11:g.27661286_27661294del	NC_000006.11:g.27661287_27661294del	NC_000006.11:g.27661288_27661294del	NC_000006.11:g.27661289_27661294del	NC_000006.11:g.27661290_27661294del	NC_000006.11:g.27661291_27661294del	NC_000006.11:g.27661292_27661294del	NC_000006.11:g.27661293_27661294del	NC_000006.11:g.27661294del	NC_000006.11:g.27661294dup	NC_000006.11:g.27661293_27661294dup	NC_000006.11:g.27661292_27661294dup	NC_000006.11:g.27661291_27661294dup	NC_000006.11:g.27661290_27661294dup	NC_000006.11:g.27661289_27661294dup	NC_000006.11:g.27661288_27661294dup	NC_000006.11:g.27661287_27661294dup	NC_000006.11:g.27661286_27661294dup	NC_000006.11:g.27661285_27661294dup	NC_000006.11:g.27661284_27661294dup	NC_000006.11:g.27661283_27661294dup	NC_000006.11:g.27661282_27661294dup	NC_000006.11:g.27661280_27661294dup	NC_000006.11:g.27661277_27661294dup	NC_000006.11:g.27661274_27661294dup

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#.

58 SubSNP, 48 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss98452413	Feb 13, 2009 (130)
2	1000GENOMES	ss1375284470	Aug 21, 2014 (142)
3	EVA_GENOME_DK	ss1578472112	Apr 01, 2015 (144)
4	SWEGEN	ss2998721140	Nov 08, 2017 (151)
5	EVA_DECODE	ss3716831558	Jul 13, 2019 (153)
6	EVA_DECODE	ss3716831559	Jul 13, 2019 (153)
7	EVA_DECODE	ss3716831560	Jul 13, 2019 (153)
8	EVA_DECODE	ss3716831561	Jul 13, 2019 (153)
9	ACPOP	ss3733315212	Jul 13, 2019 (153)
10	KHV_HUMAN_GENOMES	ss3807927278	Jul 13, 2019 (153)
11	GNOMAD	ss4138939567	Apr 26, 2021 (155)
12	GNOMAD	ss4138939568	Apr 26, 2021 (155)
13	GNOMAD	ss4138939570	Apr 26, 2021 (155)
14	GNOMAD	ss4138939571	Apr 26, 2021 (155)
15	GNOMAD	ss4138939572	Apr 26, 2021 (155)
16	GNOMAD	ss4138939573	Apr 26, 2021 (155)
17	GNOMAD	ss4138939574	Apr 26, 2021 (155)
18	GNOMAD	ss4138939575	Apr 26, 2021 (155)
19	GNOMAD	ss4138939576	Apr 26, 2021 (155)
20	GNOMAD	ss4138939577	Apr 26, 2021 (155)
21	GNOMAD	ss4138939578	Apr 26, 2021 (155)
22	GNOMAD	ss4138939579	Apr 26, 2021 (155)
23	GNOMAD	ss4138939580	Apr 26, 2021 (155)
24	GNOMAD	ss4138939581	Apr 26, 2021 (155)
25	GNOMAD	ss4138939582	Apr 26, 2021 (155)
26	GNOMAD	ss4138939583	Apr 26, 2021 (155)
27	GNOMAD	ss4138939584	Apr 26, 2021 (155)
28	GNOMAD	ss4138939585	Apr 26, 2021 (155)
29	GNOMAD	ss4138939586	Apr 26, 2021 (155)
30	GNOMAD	ss4138939587	Apr 26, 2021 (155)
31	GNOMAD	ss4138939588	Apr 26, 2021 (155)
32	GNOMAD	ss4138939589	Apr 26, 2021 (155)
33	GNOMAD	ss4138939590	Apr 26, 2021 (155)
34	GNOMAD	ss4138939591	Apr 26, 2021 (155)
35	GNOMAD	ss4138939592	Apr 26, 2021 (155)
36	GNOMAD	ss4138939593	Apr 26, 2021 (155)
37	GNOMAD	ss4138939594	Apr 26, 2021 (155)
38	GNOMAD	ss4138939595	Apr 26, 2021 (155)
39	GNOMAD	ss4138939596	Apr 26, 2021 (155)
40	GNOMAD	ss4138939597	Apr 26, 2021 (155)
41	GNOMAD	ss4138939598	Apr 26, 2021 (155)
42	GNOMAD	ss4138939599	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5176696281	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5176696282	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5176696283	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5176696284	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5176696285	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5176696286	Apr 26, 2021 (155)
49	HUGCELL_USP	ss5465578856	Oct 13, 2022 (156)
50	HUGCELL_USP	ss5465578857	Oct 13, 2022 (156)
51	HUGCELL_USP	ss5465578858	Oct 13, 2022 (156)
52	HUGCELL_USP	ss5465578859	Oct 13, 2022 (156)
53	TOMMO_GENOMICS	ss5714513298	Oct 13, 2022 (156)
54	TOMMO_GENOMICS	ss5714513299	Oct 13, 2022 (156)
55	TOMMO_GENOMICS	ss5714513300	Oct 13, 2022 (156)
56	TOMMO_GENOMICS	ss5714513301	Oct 13, 2022 (156)
57	TOMMO_GENOMICS	ss5714513302	Oct 13, 2022 (156)
58	TOMMO_GENOMICS	ss5714513303	Oct 13, 2022 (156)
59	1000Genomes	NC_000006.11 - 27661267	Oct 12, 2018 (152)
60	The Danish reference pan genome	NC_000006.11 - 27661267	Apr 26, 2020 (154)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 220479150 (NC_000006.12:27693487::T 4219/55102) Row 220479151 (NC_000006.12:27693487::TT 254/55138) Row 220479153 (NC_000006.12:27693487::TTT 502/55124)...	-	Apr 26, 2021 (155)
93	Northern Sweden	NC_000006.11 - 27661267	Jul 13, 2019 (153)
94	8.3KJPN Submission ignored due to conflicting rows: Row 34665588 (NC_000006.11:27661266:TTTTTTTTTTT: 149/15796) Row 34665589 (NC_000006.11:27661266:TTTTTTTTTT: 2407/15796) Row 34665590 (NC_000006.11:27661266:TTTTTTTTT: 196/15796)...	-	Apr 26, 2021 (155)
95	8.3KJPN Submission ignored due to conflicting rows: Row 34665588 (NC_000006.11:27661266:TTTTTTTTTTT: 149/15796) Row 34665589 (NC_000006.11:27661266:TTTTTTTTTT: 2407/15796) Row 34665590 (NC_000006.11:27661266:TTTTTTTTT: 196/15796)...	-	Apr 26, 2021 (155)
96	8.3KJPN Submission ignored due to conflicting rows: Row 34665588 (NC_000006.11:27661266:TTTTTTTTTTT: 149/15796) Row 34665589 (NC_000006.11:27661266:TTTTTTTTTT: 2407/15796) Row 34665590 (NC_000006.11:27661266:TTTTTTTTT: 196/15796)...	-	Apr 26, 2021 (155)
97	8.3KJPN Submission ignored due to conflicting rows: Row 34665588 (NC_000006.11:27661266:TTTTTTTTTTT: 149/15796) Row 34665589 (NC_000006.11:27661266:TTTTTTTTTT: 2407/15796) Row 34665590 (NC_000006.11:27661266:TTTTTTTTT: 196/15796)...	-	Apr 26, 2021 (155)
98	8.3KJPN Submission ignored due to conflicting rows: Row 34665588 (NC_000006.11:27661266:TTTTTTTTTTT: 149/15796) Row 34665589 (NC_000006.11:27661266:TTTTTTTTTT: 2407/15796) Row 34665590 (NC_000006.11:27661266:TTTTTTTTT: 196/15796)...	-	Apr 26, 2021 (155)
99	8.3KJPN Submission ignored due to conflicting rows: Row 34665588 (NC_000006.11:27661266:TTTTTTTTTTT: 149/15796) Row 34665589 (NC_000006.11:27661266:TTTTTTTTTT: 2407/15796) Row 34665590 (NC_000006.11:27661266:TTTTTTTTT: 196/15796)...	-	Apr 26, 2021 (155)
100	14KJPN Submission ignored due to conflicting rows: Row 48350402 (NC_000006.12:27693487:TTTTTTTTTT: 4512/23190) Row 48350403 (NC_000006.12:27693487:TTTTTTTTTTT: 321/23190) Row 48350404 (NC_000006.12:27693487:TTTTTTTTT: 320/23190)...	-	Oct 13, 2022 (156)
101	14KJPN Submission ignored due to conflicting rows: Row 48350402 (NC_000006.12:27693487:TTTTTTTTTT: 4512/23190) Row 48350403 (NC_000006.12:27693487:TTTTTTTTTTT: 321/23190) Row 48350404 (NC_000006.12:27693487:TTTTTTTTT: 320/23190)...	-	Oct 13, 2022 (156)
102	14KJPN Submission ignored due to conflicting rows: Row 48350402 (NC_000006.12:27693487:TTTTTTTTTT: 4512/23190) Row 48350403 (NC_000006.12:27693487:TTTTTTTTTTT: 321/23190) Row 48350404 (NC_000006.12:27693487:TTTTTTTTT: 320/23190)...	-	Oct 13, 2022 (156)
103	14KJPN Submission ignored due to conflicting rows: Row 48350402 (NC_000006.12:27693487:TTTTTTTTTT: 4512/23190) Row 48350403 (NC_000006.12:27693487:TTTTTTTTTTT: 321/23190) Row 48350404 (NC_000006.12:27693487:TTTTTTTTT: 320/23190)...	-	Oct 13, 2022 (156)
104	14KJPN Submission ignored due to conflicting rows: Row 48350402 (NC_000006.12:27693487:TTTTTTTTTT: 4512/23190) Row 48350403 (NC_000006.12:27693487:TTTTTTTTTTT: 321/23190) Row 48350404 (NC_000006.12:27693487:TTTTTTTTT: 320/23190)...	-	Oct 13, 2022 (156)
105	14KJPN Submission ignored due to conflicting rows: Row 48350402 (NC_000006.12:27693487:TTTTTTTTTT: 4512/23190) Row 48350403 (NC_000006.12:27693487:TTTTTTTTTTT: 321/23190) Row 48350404 (NC_000006.12:27693487:TTTTTTTTT: 320/23190)...	-	Oct 13, 2022 (156)
106	ALFA	NC_000006.12 - 27693488	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
92232, ss1578472112	NC_000006.11:27661266:TTTTTTTTTTTT… NC_000006.11:27661266:TTTTTTTTTTTTTTTTTTTTTTTTT:	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTT	(self)
ss4138939599	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTT:	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
8004178526	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4138939598	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTT:	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
8004178526	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4138939597	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTT:	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
8004178526	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4138939596	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTT:	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
8004178526	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss2998721140	NC_000006.11:27661266:TTTTTTTTTTTT:	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4138939595	NC_000006.12:27693487:TTTTTTTTTTTT:	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
8004178526	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss5176696281	NC_000006.11:27661266:TTTTTTTTTTT:	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3716831558, ss4138939594, ss5465578859, ss5714513299	NC_000006.12:27693487:TTTTTTTTTTT:	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
8004178526	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
31206161, ss1375284470, ss5176696282	NC_000006.11:27661266:TTTTTTTTTT:	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3807927278, ss4138939593, ss5465578857, ss5714513298	NC_000006.12:27693487:TTTTTTTTTT:	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
8004178526	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3716831559	NC_000006.12:27693488:TTTTTTTTTT:	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss5176696283	NC_000006.11:27661266:TTTTTTTTT:	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4138939592, ss5465578858, ss5714513300	NC_000006.12:27693487:TTTTTTTTT:	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
8004178526	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3716831560	NC_000006.12:27693489:TTTTTTTTT:	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4138939591	NC_000006.12:27693487:TTTTTTTT:	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
8004178526	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4138939590	NC_000006.12:27693487:TTTTTTT:	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
8004178526	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4138939589	NC_000006.12:27693487:TTTTTT:	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
8004178526	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138939588	NC_000006.12:27693487:TTTTT:	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
8004178526	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138939587	NC_000006.12:27693487:TTTT:	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
8004178526	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138939586	NC_000006.12:27693487:TTT:	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
8004178526	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138939585	NC_000006.12:27693487:TT:	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
8004178526	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5176696286	NC_000006.11:27661266:T:	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138939584, ss5465578856, ss5714513303	NC_000006.12:27693487:T:	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
8004178526	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5176696284	NC_000006.11:27661266::T	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138939567, ss5714513301	NC_000006.12:27693487::T	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
8004178526	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3716831561	NC_000006.12:27693498::T	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss98452413	NT_007592.15:27601266::T	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5176696285	NC_000006.11:27661266::TT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138939568, ss5714513302	NC_000006.12:27693487::TT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
8004178526	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138939570	NC_000006.12:27693487::TTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
8004178526	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138939571	NC_000006.12:27693487::TTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
8004178526	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138939572	NC_000006.12:27693487::TTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
8004178526	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
6600077, ss3733315212	NC_000006.11:27661266::TTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138939573	NC_000006.12:27693487::TTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138939574	NC_000006.12:27693487::TTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138939575	NC_000006.12:27693487::TTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138939576	NC_000006.12:27693487::TTTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
8004178526	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138939577	NC_000006.12:27693487::TTTTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138939578	NC_000006.12:27693487::TTTTTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138939579	NC_000006.12:27693487::TTTTTTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138939580	NC_000006.12:27693487::TTTTTTTTTTT… NC_000006.12:27693487::TTTTTTTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138939581	NC_000006.12:27693487::TTTTTTTTTTT… NC_000006.12:27693487::TTTTTTTTTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138939582	NC_000006.12:27693487::TTTTTTTTTTT… NC_000006.12:27693487::TTTTTTTTTTTTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4138939583	NC_000006.12:27693487::TTTTTTTTTTT… NC_000006.12:27693487::TTTTTTTTTTTTTTTTTTTTT	NC_000006.12:27693487:TTTTTTTTTTTT… NC_000006.12:27693487:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs71546560

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

rs71546560