Name: rs3067737
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.

rs3067737

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:15442209-15442236 (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(GT)₈ / del(GT)₇ / del(GT)₅ / d…
del(GT)₈ / del(GT)₇ / del(GT)₅ / del(GT)₃ / delGTGT / delGT / dupGT / dupGTGT / dup(GT)₃ / dup(GT)₄ / dup(GT)₅ / dup(GT)₆ / dup(GT)₇ / dup(GT)₈ / dup(GT)₉ / dup(GT)₁₀ / dup(GT)₁₁ / dup(GT)₁₂
Variation Type: Indel Insertion and Deletion
Frequency: dupGT=0.05704 (586/10274, ALFA)
dupGT=0.2540 (1272/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: EAF1 : 3 Prime UTR 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	10274	GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.92009	GTGTGTGTGTGT=0.00010, GTGTGTGTGTGTGT=0.00000, GTGTGTGTGTGTGTGTGT=0.00000, GTGTGTGTGTGTGTGTGTGTGTGT=0.00000, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.00000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.05704, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.02258, GTGTGTGTGTGTGTGTGTGTGT=0.00010, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00010, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00000	0.894705	0.008147	0.097149	22
European	Sub	8888	GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.9077	GTGTGTGTGTGT=0.0001, GTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0659, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0260, GTGTGTGTGTGTGTGTGTGTGT=0.0001, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0001, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000	0.87743	0.009483	0.113087	16
African	Sub	740	GTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.000	GTGTGTGTGTGT=0.000, GTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	28	GTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	GTGTGTGTGTGT=0.00, GTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
African American	Sub	712	GTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.000	GTGTGTGTGTGT=0.000, GTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	22	GTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	GTGTGTGTGTGT=0.00, GTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	14	GTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	GTGTGTGTGTGT=0.00, GTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	8	GTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.0	GTGTGTGTGTGT=0.0, GTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	58	GTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	GTGTGTGTGTGT=0.00, GTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	314	GTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.000	GTGTGTGTGTGT=0.000, GTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	42	GTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	GTGTGTGTGTGT=0.00, GTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Other	Sub	210	GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.995	GTGTGTGTGTGT=0.000, GTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.005, GTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	10274	(GT)₁₄=0.92009	del(GT)₈=0.00010, del(GT)₇=0.00000, del(GT)₅=0.00000, del(GT)₃=0.00010, delGTGT=0.00000, delGT=0.00000, dupGT=0.05704, dupGTGT=0.02258, dup(GT)₃=0.00010, dup(GT)₄=0.00000, dup(GT)₅=0.00000, dup(GT)₆=0.00000, dup(GT)₇=0.00000, dup(GT)₈=0.00000, dup(GT)₉=0.00000, dup(GT)₁₀=0.00000, dup(GT)₁₁=0.00000, dup(GT)₁₂=0.00000
Allele Frequency Aggregator	European	Sub	8888	(GT)₁₄=0.9077	del(GT)₈=0.0001, del(GT)₇=0.0000, del(GT)₅=0.0000, del(GT)₃=0.0001, delGTGT=0.0000, delGT=0.0000, dupGT=0.0659, dupGTGT=0.0260, dup(GT)₃=0.0001, dup(GT)₄=0.0000, dup(GT)₅=0.0000, dup(GT)₆=0.0000, dup(GT)₇=0.0000, dup(GT)₈=0.0000, dup(GT)₉=0.0000, dup(GT)₁₀=0.0000, dup(GT)₁₁=0.0000, dup(GT)₁₂=0.0000
Allele Frequency Aggregator	African	Sub	740	(GT)₁₄=1.000	del(GT)₈=0.000, del(GT)₇=0.000, del(GT)₅=0.000, del(GT)₃=0.000, delGTGT=0.000, delGT=0.000, dupGT=0.000, dupGTGT=0.000, dup(GT)₃=0.000, dup(GT)₄=0.000, dup(GT)₅=0.000, dup(GT)₆=0.000, dup(GT)₇=0.000, dup(GT)₈=0.000, dup(GT)₉=0.000, dup(GT)₁₀=0.000, dup(GT)₁₁=0.000, dup(GT)₁₂=0.000
Allele Frequency Aggregator	Latin American 2	Sub	314	(GT)₁₄=1.000	del(GT)₈=0.000, del(GT)₇=0.000, del(GT)₅=0.000, del(GT)₃=0.000, delGTGT=0.000, delGT=0.000, dupGT=0.000, dupGTGT=0.000, dup(GT)₃=0.000, dup(GT)₄=0.000, dup(GT)₅=0.000, dup(GT)₆=0.000, dup(GT)₇=0.000, dup(GT)₈=0.000, dup(GT)₉=0.000, dup(GT)₁₀=0.000, dup(GT)₁₁=0.000, dup(GT)₁₂=0.000
Allele Frequency Aggregator	Other	Sub	210	(GT)₁₄=0.995	del(GT)₈=0.000, del(GT)₇=0.000, del(GT)₅=0.000, del(GT)₃=0.000, delGTGT=0.000, delGT=0.000, dupGT=0.000, dupGTGT=0.005, dup(GT)₃=0.000, dup(GT)₄=0.000, dup(GT)₅=0.000, dup(GT)₆=0.000, dup(GT)₇=0.000, dup(GT)₈=0.000, dup(GT)₉=0.000, dup(GT)₁₀=0.000, dup(GT)₁₁=0.000, dup(GT)₁₂=0.000
Allele Frequency Aggregator	Latin American 1	Sub	58	(GT)₁₄=1.00	del(GT)₈=0.00, del(GT)₇=0.00, del(GT)₅=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00, dup(GT)₆=0.00, dup(GT)₇=0.00, dup(GT)₈=0.00, dup(GT)₉=0.00, dup(GT)₁₀=0.00, dup(GT)₁₁=0.00, dup(GT)₁₂=0.00
Allele Frequency Aggregator	South Asian	Sub	42	(GT)₁₄=1.00	del(GT)₈=0.00, del(GT)₇=0.00, del(GT)₅=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00, dup(GT)₆=0.00, dup(GT)₇=0.00, dup(GT)₈=0.00, dup(GT)₉=0.00, dup(GT)₁₀=0.00, dup(GT)₁₁=0.00, dup(GT)₁₂=0.00
Allele Frequency Aggregator	Asian	Sub	22	(GT)₁₄=1.00	del(GT)₈=0.00, del(GT)₇=0.00, del(GT)₅=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00, dup(GT)₆=0.00, dup(GT)₇=0.00, dup(GT)₈=0.00, dup(GT)₉=0.00, dup(GT)₁₀=0.00, dup(GT)₁₁=0.00, dup(GT)₁₂=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupGT=0.2540
1000Genomes	African	Sub	1322	- No frequency provided	dupGT=0.2179
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupGT=0.3661
1000Genomes	Europe	Sub	1006	- No frequency provided	dupGT=0.1859
1000Genomes	South Asian	Sub	978	- No frequency provided	dupGT=0.281
1000Genomes	American	Sub	694	- No frequency provided	dupGT=0.220

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 3	NC_000003.12:g.15442209GT[6]
GRCh38.p14 chr 3	NC_000003.12:g.15442209GT[7]
GRCh38.p14 chr 3	NC_000003.12:g.15442209GT[9]
GRCh38.p14 chr 3	NC_000003.12:g.15442209GT[11]
GRCh38.p14 chr 3	NC_000003.12:g.15442209GT[12]
GRCh38.p14 chr 3	NC_000003.12:g.15442209GT[13]
GRCh38.p14 chr 3	NC_000003.12:g.15442209GT[15]
GRCh38.p14 chr 3	NC_000003.12:g.15442209GT[16]
GRCh38.p14 chr 3	NC_000003.12:g.15442209GT[17]
GRCh38.p14 chr 3	NC_000003.12:g.15442209GT[18]
GRCh38.p14 chr 3	NC_000003.12:g.15442209GT[19]
GRCh38.p14 chr 3	NC_000003.12:g.15442209GT[20]
GRCh38.p14 chr 3	NC_000003.12:g.15442209GT[21]
GRCh38.p14 chr 3	NC_000003.12:g.15442209GT[22]
GRCh38.p14 chr 3	NC_000003.12:g.15442209GT[23]
GRCh38.p14 chr 3	NC_000003.12:g.15442209GT[24]
GRCh38.p14 chr 3	NC_000003.12:g.15442209GT[25]
GRCh38.p14 chr 3	NC_000003.12:g.15442209GT[26]
GRCh37.p13 chr 3	NC_000003.11:g.15483716GT[6]
GRCh37.p13 chr 3	NC_000003.11:g.15483716GT[7]
GRCh37.p13 chr 3	NC_000003.11:g.15483716GT[9]
GRCh37.p13 chr 3	NC_000003.11:g.15483716GT[11]
GRCh37.p13 chr 3	NC_000003.11:g.15483716GT[12]
GRCh37.p13 chr 3	NC_000003.11:g.15483716GT[13]
GRCh37.p13 chr 3	NC_000003.11:g.15483716GT[15]
GRCh37.p13 chr 3	NC_000003.11:g.15483716GT[16]
GRCh37.p13 chr 3	NC_000003.11:g.15483716GT[17]
GRCh37.p13 chr 3	NC_000003.11:g.15483716GT[18]
GRCh37.p13 chr 3	NC_000003.11:g.15483716GT[19]
GRCh37.p13 chr 3	NC_000003.11:g.15483716GT[20]
GRCh37.p13 chr 3	NC_000003.11:g.15483716GT[21]
GRCh37.p13 chr 3	NC_000003.11:g.15483716GT[22]
GRCh37.p13 chr 3	NC_000003.11:g.15483716GT[23]
GRCh37.p13 chr 3	NC_000003.11:g.15483716GT[24]
GRCh37.p13 chr 3	NC_000003.11:g.15483716GT[25]
GRCh37.p13 chr 3	NC_000003.11:g.15483716GT[26]

Gene: EAF1, ELL associated factor 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
EAF1 transcript	NM_033083.7:c.3054_3081=	N/A	3 Prime UTR Variant
EAF1 transcript variant X1	XM_011534165.2:c.3054_3… XM_011534165.2:c.3054_3081=	N/A	3 Prime UTR Variant
EAF1 transcript variant X2	XM_011534166.2:c.3054_3… XM_011534166.2:c.3054_3081=	N/A	3 Prime UTR 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	(GT)₁₄=	del(GT)₈	del(GT)₇	del(GT)₅	del(GT)₃	delGTGT	delGT	dupGT	dupGTGT	dup(GT)₃	dup(GT)₄	dup(GT)₅	dup(GT)₆	dup(GT)₇	dup(GT)₈	dup(GT)₉	dup(GT)₁₀	dup(GT)₁₁	dup(GT)₁₂
GRCh38.p14 chr 3	NC_000003.12:g.15442209_15442236=	NC_000003.12:g.15442209GT[6]	NC_000003.12:g.15442209GT[7]	NC_000003.12:g.15442209GT[9]	NC_000003.12:g.15442209GT[11]	NC_000003.12:g.15442209GT[12]	NC_000003.12:g.15442209GT[13]	NC_000003.12:g.15442209GT[15]	NC_000003.12:g.15442209GT[16]	NC_000003.12:g.15442209GT[17]	NC_000003.12:g.15442209GT[18]	NC_000003.12:g.15442209GT[19]	NC_000003.12:g.15442209GT[20]	NC_000003.12:g.15442209GT[21]	NC_000003.12:g.15442209GT[22]	NC_000003.12:g.15442209GT[23]	NC_000003.12:g.15442209GT[24]	NC_000003.12:g.15442209GT[25]	NC_000003.12:g.15442209GT[26]
GRCh37.p13 chr 3	NC_000003.11:g.15483716_15483743=	NC_000003.11:g.15483716GT[6]	NC_000003.11:g.15483716GT[7]	NC_000003.11:g.15483716GT[9]	NC_000003.11:g.15483716GT[11]	NC_000003.11:g.15483716GT[12]	NC_000003.11:g.15483716GT[13]	NC_000003.11:g.15483716GT[15]	NC_000003.11:g.15483716GT[16]	NC_000003.11:g.15483716GT[17]	NC_000003.11:g.15483716GT[18]	NC_000003.11:g.15483716GT[19]	NC_000003.11:g.15483716GT[20]	NC_000003.11:g.15483716GT[21]	NC_000003.11:g.15483716GT[22]	NC_000003.11:g.15483716GT[23]	NC_000003.11:g.15483716GT[24]	NC_000003.11:g.15483716GT[25]	NC_000003.11:g.15483716GT[26]
EAF1 transcript	NM_033083.7:c.3054_3081=	NM_033083.7:c.*3054GT[6]	NM_033083.7:c.*3054GT[7]	NM_033083.7:c.*3054GT[9]	NM_033083.7:c.*3054GT[11]	NM_033083.7:c.*3054GT[12]	NM_033083.7:c.*3054GT[13]	NM_033083.7:c.*3054GT[15]	NM_033083.7:c.*3054GT[16]	NM_033083.7:c.*3054GT[17]	NM_033083.7:c.*3054GT[18]	NM_033083.7:c.*3054GT[19]	NM_033083.7:c.*3054GT[20]	NM_033083.7:c.*3054GT[21]	NM_033083.7:c.*3054GT[22]	NM_033083.7:c.*3054GT[23]	NM_033083.7:c.*3054GT[24]	NM_033083.7:c.*3054GT[25]	NM_033083.7:c.*3054GT[26]
EAF1 transcript	NM_033083.6:c.3054_3081=	NM_033083.6:c.*3054GT[6]	NM_033083.6:c.*3054GT[7]	NM_033083.6:c.*3054GT[9]	NM_033083.6:c.*3054GT[11]	NM_033083.6:c.*3054GT[12]	NM_033083.6:c.*3054GT[13]	NM_033083.6:c.*3054GT[15]	NM_033083.6:c.*3054GT[16]	NM_033083.6:c.*3054GT[17]	NM_033083.6:c.*3054GT[18]	NM_033083.6:c.*3054GT[19]	NM_033083.6:c.*3054GT[20]	NM_033083.6:c.*3054GT[21]	NM_033083.6:c.*3054GT[22]	NM_033083.6:c.*3054GT[23]	NM_033083.6:c.*3054GT[24]	NM_033083.6:c.*3054GT[25]	NM_033083.6:c.*3054GT[26]
EAF1 transcript variant X1	XM_011534165.2:c.3054_3081=	XM_011534165.2:c.*3054GT[6]	XM_011534165.2:c.*3054GT[7]	XM_011534165.2:c.*3054GT[9]	XM_011534165.2:c.*3054GT[11]	XM_011534165.2:c.*3054GT[12]	XM_011534165.2:c.*3054GT[13]	XM_011534165.2:c.*3054GT[15]	XM_011534165.2:c.*3054GT[16]	XM_011534165.2:c.*3054GT[17]	XM_011534165.2:c.*3054GT[18]	XM_011534165.2:c.*3054GT[19]	XM_011534165.2:c.*3054GT[20]	XM_011534165.2:c.*3054GT[21]	XM_011534165.2:c.*3054GT[22]	XM_011534165.2:c.*3054GT[23]	XM_011534165.2:c.*3054GT[24]	XM_011534165.2:c.*3054GT[25]	XM_011534165.2:c.*3054GT[26]
EAF1 transcript variant X2	XM_011534165.1:c.3054_3081=	XM_011534165.1:c.*3054GT[6]	XM_011534165.1:c.*3054GT[7]	XM_011534165.1:c.*3054GT[9]	XM_011534165.1:c.*3054GT[11]	XM_011534165.1:c.*3054GT[12]	XM_011534165.1:c.*3054GT[13]	XM_011534165.1:c.*3054GT[15]	XM_011534165.1:c.*3054GT[16]	XM_011534165.1:c.*3054GT[17]	XM_011534165.1:c.*3054GT[18]	XM_011534165.1:c.*3054GT[19]	XM_011534165.1:c.*3054GT[20]	XM_011534165.1:c.*3054GT[21]	XM_011534165.1:c.*3054GT[22]	XM_011534165.1:c.*3054GT[23]	XM_011534165.1:c.*3054GT[24]	XM_011534165.1:c.*3054GT[25]	XM_011534165.1:c.*3054GT[26]
EAF1 transcript variant X2	XM_011534166.2:c.3054_3081=	XM_011534166.2:c.*3054GT[6]	XM_011534166.2:c.*3054GT[7]	XM_011534166.2:c.*3054GT[9]	XM_011534166.2:c.*3054GT[11]	XM_011534166.2:c.*3054GT[12]	XM_011534166.2:c.*3054GT[13]	XM_011534166.2:c.*3054GT[15]	XM_011534166.2:c.*3054GT[16]	XM_011534166.2:c.*3054GT[17]	XM_011534166.2:c.*3054GT[18]	XM_011534166.2:c.*3054GT[19]	XM_011534166.2:c.*3054GT[20]	XM_011534166.2:c.*3054GT[21]	XM_011534166.2:c.*3054GT[22]	XM_011534166.2:c.*3054GT[23]	XM_011534166.2:c.*3054GT[24]	XM_011534166.2:c.*3054GT[25]	XM_011534166.2:c.*3054GT[26]
EAF1 transcript variant X3	XM_011534166.1:c.3054_3081=	XM_011534166.1:c.*3054GT[6]	XM_011534166.1:c.*3054GT[7]	XM_011534166.1:c.*3054GT[9]	XM_011534166.1:c.*3054GT[11]	XM_011534166.1:c.*3054GT[12]	XM_011534166.1:c.*3054GT[13]	XM_011534166.1:c.*3054GT[15]	XM_011534166.1:c.*3054GT[16]	XM_011534166.1:c.*3054GT[17]	XM_011534166.1:c.*3054GT[18]	XM_011534166.1:c.*3054GT[19]	XM_011534166.1:c.*3054GT[20]	XM_011534166.1:c.*3054GT[21]	XM_011534166.1:c.*3054GT[22]	XM_011534166.1:c.*3054GT[23]	XM_011534166.1:c.*3054GT[24]	XM_011534166.1:c.*3054GT[25]	XM_011534166.1:c.*3054GT[26]

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#.

77 SubSNP, 40 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss4299097	Jan 05, 2002 (102)
2	HGSV	ss81158218	Dec 16, 2007 (130)
3	1000GENOMES	ss326342571	May 09, 2011 (134)
4	1000GENOMES	ss326364684	May 09, 2011 (134)
5	1000GENOMES	ss326471029	May 09, 2011 (136)
6	LUNTER	ss551210182	Apr 25, 2013 (138)
7	LUNTER	ss551286479	Apr 25, 2013 (138)
8	LUNTER	ss553001280	Apr 25, 2013 (138)
9	SSMP	ss663369461	Apr 01, 2015 (144)
10	BILGI_BIOE	ss666198058	Apr 25, 2013 (138)
11	1000GENOMES	ss1370020178	Aug 21, 2014 (142)
12	DDI	ss1536343127	Apr 01, 2015 (144)
13	EVA_UK10K_TWINSUK	ss1703523780	Apr 01, 2015 (144)
14	EVA_UK10K_TWINSUK	ss1703523782	Apr 01, 2015 (144)
15	EVA_UK10K_ALSPAC	ss1703523787	Apr 01, 2015 (144)
16	EVA_UK10K_ALSPAC	ss1703523789	Apr 01, 2015 (144)
17	TMC_SNPDB	ss1997155399	Jul 19, 2016 (147)
18	SWEGEN	ss2991879531	Jan 10, 2018 (151)
19	MCHAISSO	ss3064897812	Nov 08, 2017 (151)
20	MCHAISSO	ss3065868719	Nov 08, 2017 (151)
21	EVA_DECODE	ss3708699014	Jul 13, 2019 (153)
22	EVA_DECODE	ss3708699015	Jul 13, 2019 (153)
23	EVA_DECODE	ss3708699016	Jul 13, 2019 (153)
24	EVA_DECODE	ss3708699017	Jul 13, 2019 (153)
25	EVA_DECODE	ss3708699018	Jul 13, 2019 (153)
26	ACPOP	ss3729658752	Jul 13, 2019 (153)
27	ACPOP	ss3729658753	Jul 13, 2019 (153)
28	PACBIO	ss3784243595	Jul 13, 2019 (153)
29	PACBIO	ss3789771011	Jul 13, 2019 (153)
30	PACBIO	ss3794644769	Jul 13, 2019 (153)
31	KHV_HUMAN_GENOMES	ss3802849224	Jul 13, 2019 (153)
32	KHV_HUMAN_GENOMES	ss3802849225	Jul 13, 2019 (153)
33	EVA	ss3827677145	Apr 25, 2020 (154)
34	GNOMAD	ss4066364429	Apr 27, 2021 (155)
35	GNOMAD	ss4066364430	Apr 27, 2021 (155)
36	GNOMAD	ss4066364431	Apr 27, 2021 (155)
37	GNOMAD	ss4066364432	Apr 27, 2021 (155)
38	GNOMAD	ss4066364433	Apr 27, 2021 (155)
39	GNOMAD	ss4066364434	Apr 27, 2021 (155)
40	GNOMAD	ss4066364435	Apr 27, 2021 (155)
41	GNOMAD	ss4066364436	Apr 27, 2021 (155)
42	GNOMAD	ss4066364437	Apr 27, 2021 (155)
43	GNOMAD	ss4066364438	Apr 27, 2021 (155)
44	GNOMAD	ss4066364439	Apr 27, 2021 (155)
45	GNOMAD	ss4066364440	Apr 27, 2021 (155)
46	GNOMAD	ss4066364442	Apr 27, 2021 (155)
47	GNOMAD	ss4066364443	Apr 27, 2021 (155)
48	GNOMAD	ss4066364444	Apr 27, 2021 (155)
49	GNOMAD	ss4066364445	Apr 27, 2021 (155)
50	GNOMAD	ss4066364446	Apr 27, 2021 (155)
51	GNOMAD	ss4066364447	Apr 27, 2021 (155)
52	TOMMO_GENOMICS	ss5157937546	Apr 27, 2021 (155)
53	TOMMO_GENOMICS	ss5157937547	Apr 27, 2021 (155)
54	TOMMO_GENOMICS	ss5157937548	Apr 27, 2021 (155)
55	TOMMO_GENOMICS	ss5157937549	Apr 27, 2021 (155)
56	TOMMO_GENOMICS	ss5157937550	Apr 27, 2021 (155)
57	TOMMO_GENOMICS	ss5157937551	Apr 27, 2021 (155)
58	1000G_HIGH_COVERAGE	ss5253156490	Oct 13, 2022 (156)
59	1000G_HIGH_COVERAGE	ss5253156491	Oct 13, 2022 (156)
60	1000G_HIGH_COVERAGE	ss5253156492	Oct 13, 2022 (156)
61	1000G_HIGH_COVERAGE	ss5253156493	Oct 13, 2022 (156)
62	1000G_HIGH_COVERAGE	ss5253156494	Oct 13, 2022 (156)
63	1000G_HIGH_COVERAGE	ss5253156495	Oct 13, 2022 (156)
64	HUGCELL_USP	ss5452645645	Oct 13, 2022 (156)
65	HUGCELL_USP	ss5452645646	Oct 13, 2022 (156)
66	HUGCELL_USP	ss5452645647	Oct 13, 2022 (156)
67	HUGCELL_USP	ss5452645648	Oct 13, 2022 (156)
68	HUGCELL_USP	ss5452645649	Oct 13, 2022 (156)
69	HUGCELL_USP	ss5452645650	Oct 13, 2022 (156)
70	TOMMO_GENOMICS	ss5689246145	Oct 13, 2022 (156)
71	TOMMO_GENOMICS	ss5689246146	Oct 13, 2022 (156)
72	TOMMO_GENOMICS	ss5689246147	Oct 13, 2022 (156)
73	TOMMO_GENOMICS	ss5689246148	Oct 13, 2022 (156)
74	TOMMO_GENOMICS	ss5689246149	Oct 13, 2022 (156)
75	TOMMO_GENOMICS	ss5689246150	Oct 13, 2022 (156)
76	EVA	ss5825388456	Oct 13, 2022 (156)
77	EVA	ss5825388457	Oct 13, 2022 (156)
78	1000Genomes	NC_000003.11 - 15483716	Oct 12, 2018 (152)
79	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 7805819 (NC_000003.11:15483715::GT 678/3854) Row 7805820 (NC_000003.11:15483715::GTGT 190/3854)	-	Oct 12, 2018 (152)
80	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 7805819 (NC_000003.11:15483715::GT 678/3854) Row 7805820 (NC_000003.11:15483715::GTGT 190/3854)	-	Oct 12, 2018 (152)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99908794 (NC_000003.12:15442208::GT 23893/135876) Row 99908795 (NC_000003.12:15442208::GTGT 16211/135950) Row 99908796 (NC_000003.12:15442208::GTGTGT 1040/136004)...	-	Apr 27, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99908794 (NC_000003.12:15442208::GT 23893/135876) Row 99908795 (NC_000003.12:15442208::GTGT 16211/135950) Row 99908796 (NC_000003.12:15442208::GTGTGT 1040/136004)...	-	Apr 27, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99908794 (NC_000003.12:15442208::GT 23893/135876) Row 99908795 (NC_000003.12:15442208::GTGT 16211/135950) Row 99908796 (NC_000003.12:15442208::GTGTGT 1040/136004)...	-	Apr 27, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99908794 (NC_000003.12:15442208::GT 23893/135876) Row 99908795 (NC_000003.12:15442208::GTGT 16211/135950) Row 99908796 (NC_000003.12:15442208::GTGTGT 1040/136004)...	-	Apr 27, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99908794 (NC_000003.12:15442208::GT 23893/135876) Row 99908795 (NC_000003.12:15442208::GTGT 16211/135950) Row 99908796 (NC_000003.12:15442208::GTGTGT 1040/136004)...	-	Apr 27, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99908794 (NC_000003.12:15442208::GT 23893/135876) Row 99908795 (NC_000003.12:15442208::GTGT 16211/135950) Row 99908796 (NC_000003.12:15442208::GTGTGT 1040/136004)...	-	Apr 27, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99908794 (NC_000003.12:15442208::GT 23893/135876) Row 99908795 (NC_000003.12:15442208::GTGT 16211/135950) Row 99908796 (NC_000003.12:15442208::GTGTGT 1040/136004)...	-	Apr 27, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99908794 (NC_000003.12:15442208::GT 23893/135876) Row 99908795 (NC_000003.12:15442208::GTGT 16211/135950) Row 99908796 (NC_000003.12:15442208::GTGTGT 1040/136004)...	-	Apr 27, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99908794 (NC_000003.12:15442208::GT 23893/135876) Row 99908795 (NC_000003.12:15442208::GTGT 16211/135950) Row 99908796 (NC_000003.12:15442208::GTGTGT 1040/136004)...	-	Apr 27, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99908794 (NC_000003.12:15442208::GT 23893/135876) Row 99908795 (NC_000003.12:15442208::GTGT 16211/135950) Row 99908796 (NC_000003.12:15442208::GTGTGT 1040/136004)...	-	Apr 27, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99908794 (NC_000003.12:15442208::GT 23893/135876) Row 99908795 (NC_000003.12:15442208::GTGT 16211/135950) Row 99908796 (NC_000003.12:15442208::GTGTGT 1040/136004)...	-	Apr 27, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99908794 (NC_000003.12:15442208::GT 23893/135876) Row 99908795 (NC_000003.12:15442208::GTGT 16211/135950) Row 99908796 (NC_000003.12:15442208::GTGTGT 1040/136004)...	-	Apr 27, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99908794 (NC_000003.12:15442208::GT 23893/135876) Row 99908795 (NC_000003.12:15442208::GTGT 16211/135950) Row 99908796 (NC_000003.12:15442208::GTGTGT 1040/136004)...	-	Apr 27, 2021 (155)
94	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99908794 (NC_000003.12:15442208::GT 23893/135876) Row 99908795 (NC_000003.12:15442208::GTGT 16211/135950) Row 99908796 (NC_000003.12:15442208::GTGTGT 1040/136004)...	-	Apr 27, 2021 (155)
95	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99908794 (NC_000003.12:15442208::GT 23893/135876) Row 99908795 (NC_000003.12:15442208::GTGT 16211/135950) Row 99908796 (NC_000003.12:15442208::GTGTGT 1040/136004)...	-	Apr 27, 2021 (155)
96	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99908794 (NC_000003.12:15442208::GT 23893/135876) Row 99908795 (NC_000003.12:15442208::GTGT 16211/135950) Row 99908796 (NC_000003.12:15442208::GTGTGT 1040/136004)...	-	Apr 27, 2021 (155)
97	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99908794 (NC_000003.12:15442208::GT 23893/135876) Row 99908795 (NC_000003.12:15442208::GTGT 16211/135950) Row 99908796 (NC_000003.12:15442208::GTGTGT 1040/136004)...	-	Apr 27, 2021 (155)
98	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99908794 (NC_000003.12:15442208::GT 23893/135876) Row 99908795 (NC_000003.12:15442208::GTGT 16211/135950) Row 99908796 (NC_000003.12:15442208::GTGTGT 1040/136004)...	-	Apr 27, 2021 (155)
99	Northern Sweden Submission ignored due to conflicting rows: Row 2943617 (NC_000003.11:15483715::GT 63/600) Row 2943618 (NC_000003.11:15483715::GTGT 35/600)	-	Jul 13, 2019 (153)
100	Northern Sweden Submission ignored due to conflicting rows: Row 2943617 (NC_000003.11:15483715::GT 63/600) Row 2943618 (NC_000003.11:15483715::GTGT 35/600)	-	Jul 13, 2019 (153)
101	8.3KJPN Submission ignored due to conflicting rows: Row 15906853 (NC_000003.11:15483715::GT 5441/16760) Row 15906854 (NC_000003.11:15483715::GTGT 1104/16760) Row 15906855 (NC_000003.11:15483715:GT: 19/16760)...	-	Apr 27, 2021 (155)
102	8.3KJPN Submission ignored due to conflicting rows: Row 15906853 (NC_000003.11:15483715::GT 5441/16760) Row 15906854 (NC_000003.11:15483715::GTGT 1104/16760) Row 15906855 (NC_000003.11:15483715:GT: 19/16760)...	-	Apr 27, 2021 (155)
103	8.3KJPN Submission ignored due to conflicting rows: Row 15906853 (NC_000003.11:15483715::GT 5441/16760) Row 15906854 (NC_000003.11:15483715::GTGT 1104/16760) Row 15906855 (NC_000003.11:15483715:GT: 19/16760)...	-	Apr 27, 2021 (155)
104	8.3KJPN Submission ignored due to conflicting rows: Row 15906853 (NC_000003.11:15483715::GT 5441/16760) Row 15906854 (NC_000003.11:15483715::GTGT 1104/16760) Row 15906855 (NC_000003.11:15483715:GT: 19/16760)...	-	Apr 27, 2021 (155)
105	8.3KJPN Submission ignored due to conflicting rows: Row 15906853 (NC_000003.11:15483715::GT 5441/16760) Row 15906854 (NC_000003.11:15483715::GTGT 1104/16760) Row 15906855 (NC_000003.11:15483715:GT: 19/16760)...	-	Apr 27, 2021 (155)
106	8.3KJPN Submission ignored due to conflicting rows: Row 15906853 (NC_000003.11:15483715::GT 5441/16760) Row 15906854 (NC_000003.11:15483715::GTGT 1104/16760) Row 15906855 (NC_000003.11:15483715:GT: 19/16760)...	-	Apr 27, 2021 (155)
107	14KJPN Submission ignored due to conflicting rows: Row 23083249 (NC_000003.12:15442208::GTGTGT 108/28116) Row 23083250 (NC_000003.12:15442208::GTGT 1653/28116) Row 23083251 (NC_000003.12:15442208::GT 8345/28116)...	-	Oct 13, 2022 (156)
108	14KJPN Submission ignored due to conflicting rows: Row 23083249 (NC_000003.12:15442208::GTGTGT 108/28116) Row 23083250 (NC_000003.12:15442208::GTGT 1653/28116) Row 23083251 (NC_000003.12:15442208::GT 8345/28116)...	-	Oct 13, 2022 (156)
109	14KJPN Submission ignored due to conflicting rows: Row 23083249 (NC_000003.12:15442208::GTGTGT 108/28116) Row 23083250 (NC_000003.12:15442208::GTGT 1653/28116) Row 23083251 (NC_000003.12:15442208::GT 8345/28116)...	-	Oct 13, 2022 (156)
110	14KJPN Submission ignored due to conflicting rows: Row 23083249 (NC_000003.12:15442208::GTGTGT 108/28116) Row 23083250 (NC_000003.12:15442208::GTGT 1653/28116) Row 23083251 (NC_000003.12:15442208::GT 8345/28116)...	-	Oct 13, 2022 (156)
111	14KJPN Submission ignored due to conflicting rows: Row 23083249 (NC_000003.12:15442208::GTGTGT 108/28116) Row 23083250 (NC_000003.12:15442208::GTGT 1653/28116) Row 23083251 (NC_000003.12:15442208::GT 8345/28116)...	-	Oct 13, 2022 (156)
112	14KJPN Submission ignored due to conflicting rows: Row 23083249 (NC_000003.12:15442208::GTGTGT 108/28116) Row 23083250 (NC_000003.12:15442208::GTGT 1653/28116) Row 23083251 (NC_000003.12:15442208::GT 8345/28116)...	-	Oct 13, 2022 (156)
113	UK 10K study - Twins Submission ignored due to conflicting rows: Row 7805819 (NC_000003.11:15483715::GT 620/3708) Row 7805820 (NC_000003.11:15483715::GTGT 171/3708)	-	Oct 12, 2018 (152)
114	UK 10K study - Twins Submission ignored due to conflicting rows: Row 7805819 (NC_000003.11:15483715::GT 620/3708) Row 7805820 (NC_000003.11:15483715::GTGT 171/3708)	-	Oct 12, 2018 (152)
115	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 1698766 (NC_000003.11:15483715::GTGT 9/120) Row 1698767 (NC_000003.11:15483715::GT 87/198)	-	Jul 13, 2019 (153)
116	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 1698766 (NC_000003.11:15483715::GTGT 9/120) Row 1698767 (NC_000003.11:15483715::GT 87/198)	-	Jul 13, 2019 (153)
117	ALFA	NC_000003.12 - 15442209	Apr 27, 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)
rs61461153	May 26, 2008 (130)
rs146509331	Oct 19, 2011 (136)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4066364447	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGT:	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGT	(self)
7600273467	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGT	(self)
ss4066364446	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGT:	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGT	(self)
7600273467	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGT	(self)
ss4066364445	NC_000003.12:15442208:GTGTGTGTGT:	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGT	(self)
7600273467	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGT	(self)
ss3708699018, ss4066364444	NC_000003.12:15442208:GTGTGT:	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT	(self)
7600273467	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT	(self)
ss5157937551	NC_000003.11:15483715:GTGT:	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4066364443, ss5689246150	NC_000003.12:15442208:GTGT:	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGT	(self)
7600273467	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3708699017	NC_000003.12:15442210:GTGT:	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss2991879531, ss5157937548	NC_000003.11:15483715:GT:	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4066364442, ss5452645645, ss5689246149	NC_000003.12:15442208:GT:	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
7600273467	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3708699016	NC_000003.12:15442212:GT:	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss326342571, ss326364684, ss551210182, ss553001280	NC_000003.10:15458719::GT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
14077126, ss663369461, ss666198058, ss1370020178, ss1536343127, ss1703523780, ss1703523787, ss3729658752, ss3784243595, ss3789771011, ss3794644769, ss3827677145, ss5157937546, ss5825388456	NC_000003.11:15483715::GT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3064897812, ss3802849224, ss4066364429, ss5253156490, ss5452645646, ss5689246147	NC_000003.12:15442208::GT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
7600273467	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3708699015	NC_000003.12:15442214::GT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4299097, ss81158218	NT_022517.18:15423743::GT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss326471029, ss551286479	NC_000003.10:15458719::GTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss1703523782, ss1703523789, ss1997155399, ss3729658753, ss5157937547, ss5825388457	NC_000003.11:15483715::GTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3065868719, ss3802849225, ss4066364430, ss5253156491, ss5452645647, ss5689246146	NC_000003.12:15442208::GTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
7600273467	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3708699014	NC_000003.12:15442214::GTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss5157937550	NC_000003.11:15483715::GTGTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4066364431, ss5253156493, ss5452645649, ss5689246145	NC_000003.12:15442208::GTGTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
7600273467	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss5157937549	NC_000003.11:15483715::GTGTGTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4066364432, ss5253156492, ss5452645650, ss5689246148	NC_000003.12:15442208::GTGTGTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
7600273467	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4066364433, ss5253156494, ss5452645648	NC_000003.12:15442208::GTGTGTGTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
7600273467	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4066364434	NC_000003.12:15442208::GTGTGTGTGTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
7600273467	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4066364435	NC_000003.12:15442208::GTGTGTGTGTG… NC_000003.12:15442208::GTGTGTGTGTGTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
7600273467	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4066364436	NC_000003.12:15442208::GTGTGTGTGTG… NC_000003.12:15442208::GTGTGTGTGTGTGTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
7600273467	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4066364437, ss5253156495	NC_000003.12:15442208::GTGTGTGTGTG… NC_000003.12:15442208::GTGTGTGTGTGTGTGTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
7600273467	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4066364438	NC_000003.12:15442208::GTGTGTGTGTG… NC_000003.12:15442208::GTGTGTGTGTGTGTGTGTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
7600273467	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4066364439	NC_000003.12:15442208::GTGTGTGTGTG… NC_000003.12:15442208::GTGTGTGTGTGTGTGTGTGTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
7600273467	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4066364440	NC_000003.12:15442208::GTGTGTGTGTG… NC_000003.12:15442208::GTGTGTGTGTGTGTGTGTGTGTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
7600273467	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000003.12:15442208:GTGTGTGTGTGT… NC_000003.12:15442208:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(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 rs3067737

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

rs3067737