Name: rs3222791
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.

rs3222791

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr19:998886-998924 (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(TG)₁₃ / del(TG)₁₂ / del(TG)₁₁ …
del(TG)₁₃ / del(TG)₁₂ / del(TG)₁₁ / del(TG)₁₀ / del(TG)₉ / del(TG)₈ / del(TG)₇ / del(TG)₆ / del(TG)₅ / del(TG)₄ / del(TG)₃ / delTGTG / delTG / dupTG / dupTGTG / dup(TG)₃ / dup(TG)₄ / dup(TG)₅ / dup(TG)₇
Variation Type: Indel Insertion and Deletion
Frequency: del(TG)₁₃=0.0000 (0/3876, ALFA)
del(TG)₁₂=0.0000 (0/3876, ALFA)
del(TG)₁₀=0.0000 (0/3876, ALFA) (+ 17 more)
del(TG)₉=0.0000 (0/3876, ALFA)
del(TG)₈=0.0000 (0/3876, ALFA)
del(TG)₇=0.0000 (0/3876, ALFA)
del(TG)₆=0.0000 (0/3876, ALFA)
del(TG)₅=0.0000 (0/3876, ALFA)
del(TG)₄=0.0000 (0/3876, ALFA)
del(TG)₃=0.0000 (0/3876, ALFA)
delTGTG=0.0000 (0/3876, ALFA)
delTG=0.0000 (0/3876, ALFA)
dupTG=0.0000 (0/3876, ALFA)
dupTGTG=0.0000 (0/3876, ALFA)
dup(TG)₃=0.0000 (0/3876, ALFA)
dup(TG)₄=0.0000 (0/3876, ALFA)
dup(TG)₅=0.0000 (0/3876, ALFA)
dup(TG)₇=0.0000 (0/3876, ALFA)
delTGTG=0.2948 (1136/3854, ALSPAC)
delTGTG=0.25 (10/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: GRIN3B : 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	HWEP
Total	Global	3876	GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=1.0000	GTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0000	1.0	N/A
European	Sub	2598	GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=1.0000	GTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0000	1.0	N/A
African	Sub	816	GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=1.000	GTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000	1.0	N/A
African Others	Sub	38	GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=1.00	GTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00	1.0	N/A
African American	Sub	778	GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=1.000	GTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000	1.0	N/A
Asian	Sub	46	GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=1.00	GTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00	1.0	N/A
East Asian	Sub	34	GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=1.00	GTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00	1.0	N/A
Other Asian	Sub	12	GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=1.00	GTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00	1.0	N/A
Latin American 1	Sub	40	GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=1.00	GTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00	1.0	N/A
Latin American 2	Sub	218	GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=1.000	GTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000	1.0	N/A
South Asian	Sub	24	GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=1.00	GTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00	1.0	N/A
Other	Sub	134	GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=1.000	GTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000	1.0	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	3876	(GT)₁₉G=1.0000	del(TG)₁₃=0.0000, del(TG)₁₂=0.0000, del(TG)₁₀=0.0000, del(TG)₉=0.0000, del(TG)₈=0.0000, del(TG)₇=0.0000, del(TG)₆=0.0000, del(TG)₅=0.0000, del(TG)₄=0.0000, del(TG)₃=0.0000, delTGTG=0.0000, delTG=0.0000, dupTG=0.0000, dupTGTG=0.0000, dup(TG)₃=0.0000, dup(TG)₄=0.0000, dup(TG)₅=0.0000, dup(TG)₇=0.0000
Allele Frequency Aggregator	European	Sub	2598	(GT)₁₉G=1.0000	del(TG)₁₃=0.0000, del(TG)₁₂=0.0000, del(TG)₁₀=0.0000, del(TG)₉=0.0000, del(TG)₈=0.0000, del(TG)₇=0.0000, del(TG)₆=0.0000, del(TG)₅=0.0000, del(TG)₄=0.0000, del(TG)₃=0.0000, delTGTG=0.0000, delTG=0.0000, dupTG=0.0000, dupTGTG=0.0000, dup(TG)₃=0.0000, dup(TG)₄=0.0000, dup(TG)₅=0.0000, dup(TG)₇=0.0000
Allele Frequency Aggregator	African	Sub	816	(GT)₁₉G=1.000	del(TG)₁₃=0.000, del(TG)₁₂=0.000, del(TG)₁₀=0.000, del(TG)₉=0.000, del(TG)₈=0.000, del(TG)₇=0.000, del(TG)₆=0.000, del(TG)₅=0.000, del(TG)₄=0.000, del(TG)₃=0.000, delTGTG=0.000, delTG=0.000, dupTG=0.000, dupTGTG=0.000, dup(TG)₃=0.000, dup(TG)₄=0.000, dup(TG)₅=0.000, dup(TG)₇=0.000
Allele Frequency Aggregator	Latin American 2	Sub	218	(GT)₁₉G=1.000	del(TG)₁₃=0.000, del(TG)₁₂=0.000, del(TG)₁₀=0.000, del(TG)₉=0.000, del(TG)₈=0.000, del(TG)₇=0.000, del(TG)₆=0.000, del(TG)₅=0.000, del(TG)₄=0.000, del(TG)₃=0.000, delTGTG=0.000, delTG=0.000, dupTG=0.000, dupTGTG=0.000, dup(TG)₃=0.000, dup(TG)₄=0.000, dup(TG)₅=0.000, dup(TG)₇=0.000
Allele Frequency Aggregator	Other	Sub	134	(GT)₁₉G=1.000	del(TG)₁₃=0.000, del(TG)₁₂=0.000, del(TG)₁₀=0.000, del(TG)₉=0.000, del(TG)₈=0.000, del(TG)₇=0.000, del(TG)₆=0.000, del(TG)₅=0.000, del(TG)₄=0.000, del(TG)₃=0.000, delTGTG=0.000, delTG=0.000, dupTG=0.000, dupTGTG=0.000, dup(TG)₃=0.000, dup(TG)₄=0.000, dup(TG)₅=0.000, dup(TG)₇=0.000
Allele Frequency Aggregator	Asian	Sub	46	(GT)₁₉G=1.00	del(TG)₁₃=0.00, del(TG)₁₂=0.00, del(TG)₁₀=0.00, del(TG)₉=0.00, del(TG)₈=0.00, del(TG)₇=0.00, del(TG)₆=0.00, del(TG)₅=0.00, del(TG)₄=0.00, del(TG)₃=0.00, delTGTG=0.00, delTG=0.00, dupTG=0.00, dupTGTG=0.00, dup(TG)₃=0.00, dup(TG)₄=0.00, dup(TG)₅=0.00, dup(TG)₇=0.00
Allele Frequency Aggregator	Latin American 1	Sub	40	(GT)₁₉G=1.00	del(TG)₁₃=0.00, del(TG)₁₂=0.00, del(TG)₁₀=0.00, del(TG)₉=0.00, del(TG)₈=0.00, del(TG)₇=0.00, del(TG)₆=0.00, del(TG)₅=0.00, del(TG)₄=0.00, del(TG)₃=0.00, delTGTG=0.00, delTG=0.00, dupTG=0.00, dupTGTG=0.00, dup(TG)₃=0.00, dup(TG)₄=0.00, dup(TG)₅=0.00, dup(TG)₇=0.00
Allele Frequency Aggregator	South Asian	Sub	24	(GT)₁₉G=1.00	del(TG)₁₃=0.00, del(TG)₁₂=0.00, del(TG)₁₀=0.00, del(TG)₉=0.00, del(TG)₈=0.00, del(TG)₇=0.00, del(TG)₆=0.00, del(TG)₅=0.00, del(TG)₄=0.00, del(TG)₃=0.00, delTGTG=0.00, delTG=0.00, dupTG=0.00, dupTGTG=0.00, dup(TG)₃=0.00, dup(TG)₄=0.00, dup(TG)₅=0.00, dup(TG)₇=0.00
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(GT)₁₉G=0.7052	delTGTG=0.2948
The Danish reference pan genome	Danish	Study-wide	40	(GT)₁₉G=0.75	delTGTG=0.25

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 19	NC_000019.10:g.998887TG[6]
GRCh38.p14 chr 19	NC_000019.10:g.998887TG[7]
GRCh38.p14 chr 19	NC_000019.10:g.998887TG[8]
GRCh38.p14 chr 19	NC_000019.10:g.998887TG[9]
GRCh38.p14 chr 19	NC_000019.10:g.998887TG[10]
GRCh38.p14 chr 19	NC_000019.10:g.998887TG[11]
GRCh38.p14 chr 19	NC_000019.10:g.998887TG[12]
GRCh38.p14 chr 19	NC_000019.10:g.998887TG[13]
GRCh38.p14 chr 19	NC_000019.10:g.998887TG[14]
GRCh38.p14 chr 19	NC_000019.10:g.998887TG[15]
GRCh38.p14 chr 19	NC_000019.10:g.998887TG[16]
GRCh38.p14 chr 19	NC_000019.10:g.998887TG[17]
GRCh38.p14 chr 19	NC_000019.10:g.998887TG[18]
GRCh38.p14 chr 19	NC_000019.10:g.998887TG[20]
GRCh38.p14 chr 19	NC_000019.10:g.998887TG[21]
GRCh38.p14 chr 19	NC_000019.10:g.998887TG[22]
GRCh38.p14 chr 19	NC_000019.10:g.998887TG[23]
GRCh38.p14 chr 19	NC_000019.10:g.998887TG[24]
GRCh38.p14 chr 19	NC_000019.10:g.998887TG[26]
GRCh37.p13 chr 19	NC_000019.9:g.998886TG[6]
GRCh37.p13 chr 19	NC_000019.9:g.998886TG[7]
GRCh37.p13 chr 19	NC_000019.9:g.998886TG[8]
GRCh37.p13 chr 19	NC_000019.9:g.998886TG[9]
GRCh37.p13 chr 19	NC_000019.9:g.998886TG[10]
GRCh37.p13 chr 19	NC_000019.9:g.998886TG[11]
GRCh37.p13 chr 19	NC_000019.9:g.998886TG[12]
GRCh37.p13 chr 19	NC_000019.9:g.998886TG[13]
GRCh37.p13 chr 19	NC_000019.9:g.998886TG[14]
GRCh37.p13 chr 19	NC_000019.9:g.998886TG[15]
GRCh37.p13 chr 19	NC_000019.9:g.998886TG[16]
GRCh37.p13 chr 19	NC_000019.9:g.998886TG[17]
GRCh37.p13 chr 19	NC_000019.9:g.998886TG[18]
GRCh37.p13 chr 19	NC_000019.9:g.998886TG[20]
GRCh37.p13 chr 19	NC_000019.9:g.998886TG[21]
GRCh37.p13 chr 19	NC_000019.9:g.998886TG[22]
GRCh37.p13 chr 19	NC_000019.9:g.998886TG[23]
GRCh37.p13 chr 19	NC_000019.9:g.998886TG[24]
GRCh37.p13 chr 19	NC_000019.9:g.998886TG[26]

Gene: GRIN3B, glutamate ionotropic receptor NMDA type subunit 3B (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
GRIN3B transcript	NM_138690.3:c.	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	(GT)₁₉G=	del(TG)₁₃	del(TG)₁₂	del(TG)₁₁	del(TG)₁₀	del(TG)₉	del(TG)₈	del(TG)₇	del(TG)₆	del(TG)₅	del(TG)₄	del(TG)₃	delTGTG	delTG	dupTG	dupTGTG	dup(TG)₃	dup(TG)₄	dup(TG)₅	dup(TG)₇
GRCh38.p14 chr 19	NC_000019.10:g.998886_998924=	NC_000019.10:g.998887TG[6]	NC_000019.10:g.998887TG[7]	NC_000019.10:g.998887TG[8]	NC_000019.10:g.998887TG[9]	NC_000019.10:g.998887TG[10]	NC_000019.10:g.998887TG[11]	NC_000019.10:g.998887TG[12]	NC_000019.10:g.998887TG[13]	NC_000019.10:g.998887TG[14]	NC_000019.10:g.998887TG[15]	NC_000019.10:g.998887TG[16]	NC_000019.10:g.998887TG[17]	NC_000019.10:g.998887TG[18]	NC_000019.10:g.998887TG[20]	NC_000019.10:g.998887TG[21]	NC_000019.10:g.998887TG[22]	NC_000019.10:g.998887TG[23]	NC_000019.10:g.998887TG[24]	NC_000019.10:g.998887TG[26]
GRCh37.p13 chr 19	NC_000019.9:g.998885_998923=	NC_000019.9:g.998886TG[6]	NC_000019.9:g.998886TG[7]	NC_000019.9:g.998886TG[8]	NC_000019.9:g.998886TG[9]	NC_000019.9:g.998886TG[10]	NC_000019.9:g.998886TG[11]	NC_000019.9:g.998886TG[12]	NC_000019.9:g.998886TG[13]	NC_000019.9:g.998886TG[14]	NC_000019.9:g.998886TG[15]	NC_000019.9:g.998886TG[16]	NC_000019.9:g.998886TG[17]	NC_000019.9:g.998886TG[18]	NC_000019.9:g.998886TG[20]	NC_000019.9:g.998886TG[21]	NC_000019.9:g.998886TG[22]	NC_000019.9:g.998886TG[23]	NC_000019.9:g.998886TG[24]	NC_000019.9:g.998886TG[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#.

60 SubSNP, 42 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	GENETHON	ss4914593	Jul 13, 2002 (106)
2	LUNTER	ss552597764	Apr 25, 2013 (138)
3	LUNTER	ss552976294	Apr 25, 2013 (138)
4	SSMP	ss664460319	Apr 01, 2015 (144)
5	EVA_GENOME_DK	ss1575213700	Apr 01, 2015 (144)
6	EVA_UK10K_ALSPAC	ss1709088401	Apr 01, 2015 (144)
7	EVA_UK10K_TWINSUK	ss1709088492	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1710774421	Apr 01, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1710774422	Apr 01, 2015 (144)
10	EVA_DECODE	ss3702169304	Jul 13, 2019 (153)
11	EVA_DECODE	ss3702169305	Jul 13, 2019 (153)
12	EVA_DECODE	ss3702169306	Jul 13, 2019 (153)
13	EVA_DECODE	ss3702169308	Jul 13, 2019 (153)
14	ACPOP	ss3742780532	Jul 13, 2019 (153)
15	ACPOP	ss3742780533	Jul 13, 2019 (153)
16	ACPOP	ss3742780534	Jul 13, 2019 (153)
17	ACPOP	ss3742780535	Jul 13, 2019 (153)
18	EVA	ss3835306991	Apr 27, 2020 (154)
19	KOGIC	ss3980630657	Apr 27, 2020 (154)
20	KOGIC	ss3980630658	Apr 27, 2020 (154)
21	KOGIC	ss3980630659	Apr 27, 2020 (154)
22	KOGIC	ss3980630660	Apr 27, 2020 (154)
23	KOGIC	ss3980630661	Apr 27, 2020 (154)
24	KOGIC	ss3980630662	Apr 27, 2020 (154)
25	GNOMAD	ss4326255579	Apr 26, 2021 (155)
26	GNOMAD	ss4326255580	Apr 26, 2021 (155)
27	GNOMAD	ss4326255581	Apr 26, 2021 (155)
28	GNOMAD	ss4326255582	Apr 26, 2021 (155)
29	GNOMAD	ss4326255583	Apr 26, 2021 (155)
30	GNOMAD	ss4326255589	Apr 26, 2021 (155)
31	GNOMAD	ss4326255590	Apr 26, 2021 (155)
32	GNOMAD	ss4326255591	Apr 26, 2021 (155)
33	GNOMAD	ss4326255592	Apr 26, 2021 (155)
34	GNOMAD	ss4326255593	Apr 26, 2021 (155)
35	GNOMAD	ss4326255594	Apr 26, 2021 (155)
36	GNOMAD	ss4326255595	Apr 26, 2021 (155)
37	GNOMAD	ss4326255596	Apr 26, 2021 (155)
38	GNOMAD	ss4326255597	Apr 26, 2021 (155)
39	GNOMAD	ss4326255598	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5226319068	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5226319069	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5226319070	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5226319071	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5226319072	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5226319073	Apr 26, 2021 (155)
46	1000G_HIGH_COVERAGE	ss5306184172	Oct 16, 2022 (156)
47	HUGCELL_USP	ss5498861231	Oct 16, 2022 (156)
48	HUGCELL_USP	ss5498861232	Oct 16, 2022 (156)
49	HUGCELL_USP	ss5498861233	Oct 16, 2022 (156)
50	HUGCELL_USP	ss5498861234	Oct 16, 2022 (156)
51	HUGCELL_USP	ss5498861235	Oct 16, 2022 (156)
52	HUGCELL_USP	ss5498861236	Oct 16, 2022 (156)
53	TOMMO_GENOMICS	ss5784447946	Oct 16, 2022 (156)
54	TOMMO_GENOMICS	ss5784447947	Oct 16, 2022 (156)
55	TOMMO_GENOMICS	ss5784447948	Oct 16, 2022 (156)
56	TOMMO_GENOMICS	ss5784447949	Oct 16, 2022 (156)
57	TOMMO_GENOMICS	ss5784447950	Oct 16, 2022 (156)
58	TOMMO_GENOMICS	ss5784447951	Oct 16, 2022 (156)
59	EVA	ss5840136753	Oct 16, 2022 (156)
60	EVA	ss5840136754	Oct 16, 2022 (156)
61	The Avon Longitudinal Study of Parents and Children	NC_000019.9 - 998885	Oct 12, 2018 (152)
62	The Danish reference pan genome	NC_000019.9 - 998885	Apr 27, 2020 (154)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 531703182 (NC_000019.10:998885::GT 5727/115344) Row 531703183 (NC_000019.10:998885::GTGT 1161/115402) Row 531703184 (NC_000019.10:998885::GTGTGT 215/115416)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 531703182 (NC_000019.10:998885::GT 5727/115344) Row 531703183 (NC_000019.10:998885::GTGT 1161/115402) Row 531703184 (NC_000019.10:998885::GTGTGT 215/115416)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 531703182 (NC_000019.10:998885::GT 5727/115344) Row 531703183 (NC_000019.10:998885::GTGT 1161/115402) Row 531703184 (NC_000019.10:998885::GTGTGT 215/115416)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 531703182 (NC_000019.10:998885::GT 5727/115344) Row 531703183 (NC_000019.10:998885::GTGT 1161/115402) Row 531703184 (NC_000019.10:998885::GTGTGT 215/115416)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 531703182 (NC_000019.10:998885::GT 5727/115344) Row 531703183 (NC_000019.10:998885::GTGT 1161/115402) Row 531703184 (NC_000019.10:998885::GTGTGT 215/115416)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 531703182 (NC_000019.10:998885::GT 5727/115344) Row 531703183 (NC_000019.10:998885::GTGT 1161/115402) Row 531703184 (NC_000019.10:998885::GTGTGT 215/115416)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 531703182 (NC_000019.10:998885::GT 5727/115344) Row 531703183 (NC_000019.10:998885::GTGT 1161/115402) Row 531703184 (NC_000019.10:998885::GTGTGT 215/115416)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 531703182 (NC_000019.10:998885::GT 5727/115344) Row 531703183 (NC_000019.10:998885::GTGT 1161/115402) Row 531703184 (NC_000019.10:998885::GTGTGT 215/115416)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 531703182 (NC_000019.10:998885::GT 5727/115344) Row 531703183 (NC_000019.10:998885::GTGT 1161/115402) Row 531703184 (NC_000019.10:998885::GTGTGT 215/115416)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 531703182 (NC_000019.10:998885::GT 5727/115344) Row 531703183 (NC_000019.10:998885::GTGT 1161/115402) Row 531703184 (NC_000019.10:998885::GTGTGT 215/115416)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 531703182 (NC_000019.10:998885::GT 5727/115344) Row 531703183 (NC_000019.10:998885::GTGT 1161/115402) Row 531703184 (NC_000019.10:998885::GTGTGT 215/115416)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 531703182 (NC_000019.10:998885::GT 5727/115344) Row 531703183 (NC_000019.10:998885::GTGT 1161/115402) Row 531703184 (NC_000019.10:998885::GTGTGT 215/115416)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 531703182 (NC_000019.10:998885::GT 5727/115344) Row 531703183 (NC_000019.10:998885::GTGT 1161/115402) Row 531703184 (NC_000019.10:998885::GTGTGT 215/115416)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 531703182 (NC_000019.10:998885::GT 5727/115344) Row 531703183 (NC_000019.10:998885::GTGT 1161/115402) Row 531703184 (NC_000019.10:998885::GTGTGT 215/115416)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 531703182 (NC_000019.10:998885::GT 5727/115344) Row 531703183 (NC_000019.10:998885::GTGT 1161/115402) Row 531703184 (NC_000019.10:998885::GTGTGT 215/115416)...	-	Apr 26, 2021 (155)
78	Korean Genome Project Submission ignored due to conflicting rows: Row 37008658 (NC_000019.10:998897:GTGT: 453/1832) Row 37008659 (NC_000019.10:998899:GT: 288/1832) Row 37008660 (NC_000019.10:998885:GTGTGTGTGTGTGTGT: 26/1832)...	-	Apr 27, 2020 (154)
79	Korean Genome Project Submission ignored due to conflicting rows: Row 37008658 (NC_000019.10:998897:GTGT: 453/1832) Row 37008659 (NC_000019.10:998899:GT: 288/1832) Row 37008660 (NC_000019.10:998885:GTGTGTGTGTGTGTGT: 26/1832)...	-	Apr 27, 2020 (154)
80	Korean Genome Project Submission ignored due to conflicting rows: Row 37008658 (NC_000019.10:998897:GTGT: 453/1832) Row 37008659 (NC_000019.10:998899:GT: 288/1832) Row 37008660 (NC_000019.10:998885:GTGTGTGTGTGTGTGT: 26/1832)...	-	Apr 27, 2020 (154)
81	Korean Genome Project Submission ignored due to conflicting rows: Row 37008658 (NC_000019.10:998897:GTGT: 453/1832) Row 37008659 (NC_000019.10:998899:GT: 288/1832) Row 37008660 (NC_000019.10:998885:GTGTGTGTGTGTGTGT: 26/1832)...	-	Apr 27, 2020 (154)
82	Korean Genome Project Submission ignored due to conflicting rows: Row 37008658 (NC_000019.10:998897:GTGT: 453/1832) Row 37008659 (NC_000019.10:998899:GT: 288/1832) Row 37008660 (NC_000019.10:998885:GTGTGTGTGTGTGTGT: 26/1832)...	-	Apr 27, 2020 (154)
83	Korean Genome Project Submission ignored due to conflicting rows: Row 37008658 (NC_000019.10:998897:GTGT: 453/1832) Row 37008659 (NC_000019.10:998899:GT: 288/1832) Row 37008660 (NC_000019.10:998885:GTGTGTGTGTGTGTGT: 26/1832)...	-	Apr 27, 2020 (154)
84	Northern Sweden Submission ignored due to conflicting rows: Row 16065397 (NC_000019.9:998884:GTGT: 163/594) Row 16065398 (NC_000019.9:998884:GT: 16/594) Row 16065399 (NC_000019.9:998884::GT 9/594)...	-	Jul 13, 2019 (153)
85	Northern Sweden Submission ignored due to conflicting rows: Row 16065397 (NC_000019.9:998884:GTGT: 163/594) Row 16065398 (NC_000019.9:998884:GT: 16/594) Row 16065399 (NC_000019.9:998884::GT 9/594)...	-	Jul 13, 2019 (153)
86	Northern Sweden Submission ignored due to conflicting rows: Row 16065397 (NC_000019.9:998884:GTGT: 163/594) Row 16065398 (NC_000019.9:998884:GT: 16/594) Row 16065399 (NC_000019.9:998884::GT 9/594)...	-	Jul 13, 2019 (153)
87	Northern Sweden Submission ignored due to conflicting rows: Row 16065397 (NC_000019.9:998884:GTGT: 163/594) Row 16065398 (NC_000019.9:998884:GT: 16/594) Row 16065399 (NC_000019.9:998884::GT 9/594)...	-	Jul 13, 2019 (153)
88	8.3KJPN Submission ignored due to conflicting rows: Row 84288375 (NC_000019.9:998884:GTGT: 3941/16652) Row 84288376 (NC_000019.9:998884:GT: 2010/16652) Row 84288377 (NC_000019.9:998884::GT 206/16652)...	-	Apr 26, 2021 (155)
89	8.3KJPN Submission ignored due to conflicting rows: Row 84288375 (NC_000019.9:998884:GTGT: 3941/16652) Row 84288376 (NC_000019.9:998884:GT: 2010/16652) Row 84288377 (NC_000019.9:998884::GT 206/16652)...	-	Apr 26, 2021 (155)
90	8.3KJPN Submission ignored due to conflicting rows: Row 84288375 (NC_000019.9:998884:GTGT: 3941/16652) Row 84288376 (NC_000019.9:998884:GT: 2010/16652) Row 84288377 (NC_000019.9:998884::GT 206/16652)...	-	Apr 26, 2021 (155)
91	8.3KJPN Submission ignored due to conflicting rows: Row 84288375 (NC_000019.9:998884:GTGT: 3941/16652) Row 84288376 (NC_000019.9:998884:GT: 2010/16652) Row 84288377 (NC_000019.9:998884::GT 206/16652)...	-	Apr 26, 2021 (155)
92	8.3KJPN Submission ignored due to conflicting rows: Row 84288375 (NC_000019.9:998884:GTGT: 3941/16652) Row 84288376 (NC_000019.9:998884:GT: 2010/16652) Row 84288377 (NC_000019.9:998884::GT 206/16652)...	-	Apr 26, 2021 (155)
93	8.3KJPN Submission ignored due to conflicting rows: Row 84288375 (NC_000019.9:998884:GTGT: 3941/16652) Row 84288376 (NC_000019.9:998884:GT: 2010/16652) Row 84288377 (NC_000019.9:998884::GT 206/16652)...	-	Apr 26, 2021 (155)
94	14KJPN Submission ignored due to conflicting rows: Row 118285050 (NC_000019.10:998885:GT: 3254/28200) Row 118285051 (NC_000019.10:998885:GTGT: 6616/28200) Row 118285052 (NC_000019.10:998885::GT 310/28200)...	-	Oct 16, 2022 (156)
95	14KJPN Submission ignored due to conflicting rows: Row 118285050 (NC_000019.10:998885:GT: 3254/28200) Row 118285051 (NC_000019.10:998885:GTGT: 6616/28200) Row 118285052 (NC_000019.10:998885::GT 310/28200)...	-	Oct 16, 2022 (156)
96	14KJPN Submission ignored due to conflicting rows: Row 118285050 (NC_000019.10:998885:GT: 3254/28200) Row 118285051 (NC_000019.10:998885:GTGT: 6616/28200) Row 118285052 (NC_000019.10:998885::GT 310/28200)...	-	Oct 16, 2022 (156)
97	14KJPN Submission ignored due to conflicting rows: Row 118285050 (NC_000019.10:998885:GT: 3254/28200) Row 118285051 (NC_000019.10:998885:GTGT: 6616/28200) Row 118285052 (NC_000019.10:998885::GT 310/28200)...	-	Oct 16, 2022 (156)
98	14KJPN Submission ignored due to conflicting rows: Row 118285050 (NC_000019.10:998885:GT: 3254/28200) Row 118285051 (NC_000019.10:998885:GTGT: 6616/28200) Row 118285052 (NC_000019.10:998885::GT 310/28200)...	-	Oct 16, 2022 (156)
99	14KJPN Submission ignored due to conflicting rows: Row 118285050 (NC_000019.10:998885:GT: 3254/28200) Row 118285051 (NC_000019.10:998885:GTGT: 6616/28200) Row 118285052 (NC_000019.10:998885::GT 310/28200)...	-	Oct 16, 2022 (156)
100	UK 10K study - Twins	-	Oct 12, 2018 (152)
101	UK 10K study - Twins Submission ignored due to conflicting rows: Row 41795059 (NC_000019.9:998884:GTGT: 1056/3708) Row 41795060 (NC_000019.9:998886:GT: 144/3708)	-	Apr 27, 2020 (154)
102	ALFA	NC_000019.10 - 998886	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
ss4326255598	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGT:	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTG	(self)
11774277364	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTG	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTG	(self)
11774277364	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTG	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTG	(self)
ss4326255597	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGT:	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTG	(self)
ss4326255596	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGT:	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTG	(self)
11774277364	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTG	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTG	(self)
11774277364	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTG	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTG	(self)
ss5226319072	NC_000019.9:998884:GTGTGTGTGTGTGTG… NC_000019.9:998884:GTGTGTGTGTGTGTGT:	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTG	(self)
ss3702169308, ss3980630659, ss4326255595, ss5784447950	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGT:	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTG	(self)
11774277364	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTG	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTG	(self)
ss4914593	NT_011255.14:938885:TGTGTGTGTGTGTG… NT_011255.14:938885:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTG	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTG	(self)
ss4326255594	NC_000019.10:998885:GTGTGTGTGTGTGT:	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTG	(self)
11774277364	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTG	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTG	(self)
11774277364	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTG	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss4326255593	NC_000019.10:998885:GTGTGTGTGT:	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
11774277364	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTG	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss3742780535	NC_000019.9:998884:GTGTGTGT:	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss4326255592, ss5498861235	NC_000019.10:998885:GTGTGTGT:	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
11774277364	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss3980630662	NC_000019.10:998893:GTGTGTGT:	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss5226319071	NC_000019.9:998884:GTGTGT:	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss4326255591, ss5498861233, ss5784447949	NC_000019.10:998885:GTGTGT:	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
11774277364	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss3702169306, ss3980630661	NC_000019.10:998895:GTGTGT:	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss4914593	NT_011255.14:938885:TGTGTGTGTGTGTG… NT_011255.14:938885:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss552597764, ss552976294	NC_000019.8:949884:GTGT:	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
41795059, 614132, ss664460319, ss1575213700, ss1709088401, ss1709088492, ss3742780532, ss3835306991, ss5226319068, ss5840136753	NC_000019.9:998884:GTGT:	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss4326255590, ss5498861231, ss5784447947	NC_000019.10:998885:GTGT:	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
11774277364	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss3702169305, ss3980630657	NC_000019.10:998897:GTGT:	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss4914593	NT_011255.14:938885:TGTGTGTGTGTGTG… NT_011255.14:938885:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss3742780533, ss5226319069, ss5840136754	NC_000019.9:998884:GT:	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss1710774421, ss1710774422	NC_000019.9:998886:GT:	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss4326255589, ss5306184172, ss5498861232, ss5784447946	NC_000019.10:998885:GT:	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
11774277364	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss3702169304, ss3980630658	NC_000019.10:998899:GT:	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss4914593	NT_011255.14:938885:TGTGTGTGTGTGTG… NT_011255.14:938885:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss3742780534, ss5226319070	NC_000019.9:998884::GT	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss4326255579, ss5498861236, ss5784447948	NC_000019.10:998885::GT	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
11774277364	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss3980630660	NC_000019.10:998901::GT	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss5226319073	NC_000019.9:998884::GTGT	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss4326255580, ss5498861234, ss5784447951	NC_000019.10:998885::GTGT	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
11774277364	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss4326255581	NC_000019.10:998885::GTGTGT	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
11774277364	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss4326255582	NC_000019.10:998885::GTGTGTGT	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
11774277364	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss4326255583	NC_000019.10:998885::GTGTGTGTGT	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
11774277364	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
11774277364	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3285731744	NC_000019.10:998885::GTGTGTGTGTGTGT	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG
ss3285731757	NC_000019.10:998885:GTGTGTGTGTGT:	NC_000019.10:998885:GTGTGTGTGTGTGT… NC_000019.10:998885:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTG

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

No publications for rs3222791

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
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs3222791