Name: rs778856865
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.

rs778856865

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr17:71122829-71122867 (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(GA)₉ / del(GA)₈ / del(GA)₇ / d…
del(GA)₉ / del(GA)₈ / del(GA)₇ / del(GA)₆ / del(GA)₅ / del(GA)₄ / del(GA)₃ / delGAGA / delGA / dupGA / dupGAGA / dup(GA)₃ / dup(GA)₄ / dup(GA)₅ / dup(GA)₆ / dup(GA)₇ / dup(GA)₈ / dup(GA)₉ / dup(GA)₁₀ / dup(GA)₁₁ / dup(GA)₁₂ / dup(GA)₁₃ / dup(GA)₁₄ / dup(GA)₁₅
Variation Type: Indel Insertion and Deletion
Frequency: del(GA)₆=0.000045 (12/264690, TOPMED)
del(GA)₉=0.0000 (0/8408, ALFA)
del(GA)₈=0.0000 (0/8408, ALFA) (+ 16 more)
del(GA)₇=0.0000 (0/8408, ALFA)
del(GA)₆=0.0000 (0/8408, ALFA)
del(GA)₅=0.0000 (0/8408, ALFA)
del(GA)₄=0.0000 (0/8408, ALFA)
del(GA)₃=0.0000 (0/8408, ALFA)
delGAGA=0.0000 (0/8408, ALFA)
delGA=0.0000 (0/8408, ALFA)
dupGA=0.0000 (0/8408, ALFA)
dupGAGA=0.0000 (0/8408, ALFA)
dup(GA)₃=0.0000 (0/8408, ALFA)
dup(GA)₄=0.0000 (0/8408, ALFA)
dup(GA)₅=0.0000 (0/8408, ALFA)
dup(GA)₆=0.0000 (0/8408, ALFA)
dup(GA)₇=0.0000 (0/8408, ALFA)
dupGAGA=0.2317 (893/3854, ALSPAC)
dupGAGA=0.2257 (837/3708, TWINSUK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CASC17 : Intron 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	8408	AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=1.0000	AGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000	1.0	N/A
European	Sub	6314	AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=1.0000	AGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000	1.0	N/A
African	Sub	1466	AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=1.0000	AGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000	1.0	N/A
African Others	Sub	50	AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=1.00	AGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00	1.0	N/A
African American	Sub	1416	AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=1.0000	AGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000	1.0	N/A
Asian	Sub	66	AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=1.00	AGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00	1.0	N/A
East Asian	Sub	50	AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=1.00	AGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00	1.0	N/A
Other Asian	Sub	16	AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=1.00	AGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00	1.0	N/A
Latin American 1	Sub	72	AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=1.00	AGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00	1.0	N/A
Latin American 2	Sub	218	AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=1.000	AGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000	1.0	N/A
South Asian	Sub	28	AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=1.00	AGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00	1.0	N/A
Other	Sub	244	AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=1.000	AGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=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
TopMed	Global	Study-wide	264690	(AG)₁₉A=0.999955	del(GA)₆=0.000045
Allele Frequency Aggregator	Total	Global	8408	(AG)₁₉A=1.0000	del(GA)₉=0.0000, del(GA)₈=0.0000, del(GA)₇=0.0000, del(GA)₆=0.0000, del(GA)₅=0.0000, del(GA)₄=0.0000, del(GA)₃=0.0000, delGAGA=0.0000, delGA=0.0000, dupGA=0.0000, dupGAGA=0.0000, dup(GA)₃=0.0000, dup(GA)₄=0.0000, dup(GA)₅=0.0000, dup(GA)₆=0.0000, dup(GA)₇=0.0000
Allele Frequency Aggregator	European	Sub	6314	(AG)₁₉A=1.0000	del(GA)₉=0.0000, del(GA)₈=0.0000, del(GA)₇=0.0000, del(GA)₆=0.0000, del(GA)₅=0.0000, del(GA)₄=0.0000, del(GA)₃=0.0000, delGAGA=0.0000, delGA=0.0000, dupGA=0.0000, dupGAGA=0.0000, dup(GA)₃=0.0000, dup(GA)₄=0.0000, dup(GA)₅=0.0000, dup(GA)₆=0.0000, dup(GA)₇=0.0000
Allele Frequency Aggregator	African	Sub	1466	(AG)₁₉A=1.0000	del(GA)₉=0.0000, del(GA)₈=0.0000, del(GA)₇=0.0000, del(GA)₆=0.0000, del(GA)₅=0.0000, del(GA)₄=0.0000, del(GA)₃=0.0000, delGAGA=0.0000, delGA=0.0000, dupGA=0.0000, dupGAGA=0.0000, dup(GA)₃=0.0000, dup(GA)₄=0.0000, dup(GA)₅=0.0000, dup(GA)₆=0.0000, dup(GA)₇=0.0000
Allele Frequency Aggregator	Other	Sub	244	(AG)₁₉A=1.000	del(GA)₉=0.000, del(GA)₈=0.000, del(GA)₇=0.000, del(GA)₆=0.000, del(GA)₅=0.000, del(GA)₄=0.000, del(GA)₃=0.000, delGAGA=0.000, delGA=0.000, dupGA=0.000, dupGAGA=0.000, dup(GA)₃=0.000, dup(GA)₄=0.000, dup(GA)₅=0.000, dup(GA)₆=0.000, dup(GA)₇=0.000
Allele Frequency Aggregator	Latin American 2	Sub	218	(AG)₁₉A=1.000	del(GA)₉=0.000, del(GA)₈=0.000, del(GA)₇=0.000, del(GA)₆=0.000, del(GA)₅=0.000, del(GA)₄=0.000, del(GA)₃=0.000, delGAGA=0.000, delGA=0.000, dupGA=0.000, dupGAGA=0.000, dup(GA)₃=0.000, dup(GA)₄=0.000, dup(GA)₅=0.000, dup(GA)₆=0.000, dup(GA)₇=0.000
Allele Frequency Aggregator	Latin American 1	Sub	72	(AG)₁₉A=1.00	del(GA)₉=0.00, del(GA)₈=0.00, del(GA)₇=0.00, del(GA)₆=0.00, del(GA)₅=0.00, del(GA)₄=0.00, del(GA)₃=0.00, delGAGA=0.00, delGA=0.00, dupGA=0.00, dupGAGA=0.00, dup(GA)₃=0.00, dup(GA)₄=0.00, dup(GA)₅=0.00, dup(GA)₆=0.00, dup(GA)₇=0.00
Allele Frequency Aggregator	Asian	Sub	66	(AG)₁₉A=1.00	del(GA)₉=0.00, del(GA)₈=0.00, del(GA)₇=0.00, del(GA)₆=0.00, del(GA)₅=0.00, del(GA)₄=0.00, del(GA)₃=0.00, delGAGA=0.00, delGA=0.00, dupGA=0.00, dupGAGA=0.00, dup(GA)₃=0.00, dup(GA)₄=0.00, dup(GA)₅=0.00, dup(GA)₆=0.00, dup(GA)₇=0.00
Allele Frequency Aggregator	South Asian	Sub	28	(AG)₁₉A=1.00	del(GA)₉=0.00, del(GA)₈=0.00, del(GA)₇=0.00, del(GA)₆=0.00, del(GA)₅=0.00, del(GA)₄=0.00, del(GA)₃=0.00, delGAGA=0.00, delGA=0.00, dupGA=0.00, dupGAGA=0.00, dup(GA)₃=0.00, dup(GA)₄=0.00, dup(GA)₅=0.00, dup(GA)₆=0.00, dup(GA)₇=0.00
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	- No frequency provided	dupGAGA=0.2317
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	- No frequency provided	dupGAGA=0.2257

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 17	NC_000017.11:g.71122830GA[10]
GRCh38.p14 chr 17	NC_000017.11:g.71122830GA[11]
GRCh38.p14 chr 17	NC_000017.11:g.71122830GA[12]
GRCh38.p14 chr 17	NC_000017.11:g.71122830GA[13]
GRCh38.p14 chr 17	NC_000017.11:g.71122830GA[14]
GRCh38.p14 chr 17	NC_000017.11:g.71122830GA[15]
GRCh38.p14 chr 17	NC_000017.11:g.71122830GA[16]
GRCh38.p14 chr 17	NC_000017.11:g.71122830GA[17]
GRCh38.p14 chr 17	NC_000017.11:g.71122830GA[18]
GRCh38.p14 chr 17	NC_000017.11:g.71122830GA[20]
GRCh38.p14 chr 17	NC_000017.11:g.71122830GA[21]
GRCh38.p14 chr 17	NC_000017.11:g.71122830GA[22]
GRCh38.p14 chr 17	NC_000017.11:g.71122830GA[23]
GRCh38.p14 chr 17	NC_000017.11:g.71122830GA[24]
GRCh38.p14 chr 17	NC_000017.11:g.71122830GA[25]
GRCh38.p14 chr 17	NC_000017.11:g.71122830GA[26]
GRCh38.p14 chr 17	NC_000017.11:g.71122830GA[27]
GRCh38.p14 chr 17	NC_000017.11:g.71122830GA[28]
GRCh38.p14 chr 17	NC_000017.11:g.71122830GA[29]
GRCh38.p14 chr 17	NC_000017.11:g.71122830GA[30]
GRCh38.p14 chr 17	NC_000017.11:g.71122830GA[31]
GRCh38.p14 chr 17	NC_000017.11:g.71122830GA[32]
GRCh38.p14 chr 17	NC_000017.11:g.71122830GA[33]
GRCh38.p14 chr 17	NC_000017.11:g.71122830GA[34]
GRCh37.p13 chr 17	NC_000017.10:g.69118971GA[10]
GRCh37.p13 chr 17	NC_000017.10:g.69118971GA[11]
GRCh37.p13 chr 17	NC_000017.10:g.69118971GA[12]
GRCh37.p13 chr 17	NC_000017.10:g.69118971GA[13]
GRCh37.p13 chr 17	NC_000017.10:g.69118971GA[14]
GRCh37.p13 chr 17	NC_000017.10:g.69118971GA[15]
GRCh37.p13 chr 17	NC_000017.10:g.69118971GA[16]
GRCh37.p13 chr 17	NC_000017.10:g.69118971GA[17]
GRCh37.p13 chr 17	NC_000017.10:g.69118971GA[18]
GRCh37.p13 chr 17	NC_000017.10:g.69118971GA[20]
GRCh37.p13 chr 17	NC_000017.10:g.69118971GA[21]
GRCh37.p13 chr 17	NC_000017.10:g.69118971GA[22]
GRCh37.p13 chr 17	NC_000017.10:g.69118971GA[23]
GRCh37.p13 chr 17	NC_000017.10:g.69118971GA[24]
GRCh37.p13 chr 17	NC_000017.10:g.69118971GA[25]
GRCh37.p13 chr 17	NC_000017.10:g.69118971GA[26]
GRCh37.p13 chr 17	NC_000017.10:g.69118971GA[27]
GRCh37.p13 chr 17	NC_000017.10:g.69118971GA[28]
GRCh37.p13 chr 17	NC_000017.10:g.69118971GA[29]
GRCh37.p13 chr 17	NC_000017.10:g.69118971GA[30]
GRCh37.p13 chr 17	NC_000017.10:g.69118971GA[31]
GRCh37.p13 chr 17	NC_000017.10:g.69118971GA[32]
GRCh37.p13 chr 17	NC_000017.10:g.69118971GA[33]
GRCh37.p13 chr 17	NC_000017.10:g.69118971GA[34]

Gene: CASC17, cancer susceptibility 17 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CASC17 transcript	NR_104152.1:n.	N/A	Intron 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	(AG)₁₉A=	del(GA)₉	del(GA)₈	del(GA)₇	del(GA)₆	del(GA)₅	del(GA)₄	del(GA)₃	delGAGA	delGA	dupGA	dupGAGA	dup(GA)₃	dup(GA)₄	dup(GA)₅	dup(GA)₆	dup(GA)₇	dup(GA)₈	dup(GA)₉	dup(GA)₁₀	dup(GA)₁₁	dup(GA)₁₂	dup(GA)₁₃	dup(GA)₁₄	dup(GA)₁₅
GRCh38.p14 chr 17	NC_000017.11:g.71122829_71122867=	NC_000017.11:g.71122830GA[10]	NC_000017.11:g.71122830GA[11]	NC_000017.11:g.71122830GA[12]	NC_000017.11:g.71122830GA[13]	NC_000017.11:g.71122830GA[14]	NC_000017.11:g.71122830GA[15]	NC_000017.11:g.71122830GA[16]	NC_000017.11:g.71122830GA[17]	NC_000017.11:g.71122830GA[18]	NC_000017.11:g.71122830GA[20]	NC_000017.11:g.71122830GA[21]	NC_000017.11:g.71122830GA[22]	NC_000017.11:g.71122830GA[23]	NC_000017.11:g.71122830GA[24]	NC_000017.11:g.71122830GA[25]	NC_000017.11:g.71122830GA[26]	NC_000017.11:g.71122830GA[27]	NC_000017.11:g.71122830GA[28]	NC_000017.11:g.71122830GA[29]	NC_000017.11:g.71122830GA[30]	NC_000017.11:g.71122830GA[31]	NC_000017.11:g.71122830GA[32]	NC_000017.11:g.71122830GA[33]	NC_000017.11:g.71122830GA[34]
GRCh37.p13 chr 17	NC_000017.10:g.69118970_69119008=	NC_000017.10:g.69118971GA[10]	NC_000017.10:g.69118971GA[11]	NC_000017.10:g.69118971GA[12]	NC_000017.10:g.69118971GA[13]	NC_000017.10:g.69118971GA[14]	NC_000017.10:g.69118971GA[15]	NC_000017.10:g.69118971GA[16]	NC_000017.10:g.69118971GA[17]	NC_000017.10:g.69118971GA[18]	NC_000017.10:g.69118971GA[20]	NC_000017.10:g.69118971GA[21]	NC_000017.10:g.69118971GA[22]	NC_000017.10:g.69118971GA[23]	NC_000017.10:g.69118971GA[24]	NC_000017.10:g.69118971GA[25]	NC_000017.10:g.69118971GA[26]	NC_000017.10:g.69118971GA[27]	NC_000017.10:g.69118971GA[28]	NC_000017.10:g.69118971GA[29]	NC_000017.10:g.69118971GA[30]	NC_000017.10:g.69118971GA[31]	NC_000017.10:g.69118971GA[32]	NC_000017.10:g.69118971GA[33]	NC_000017.10:g.69118971GA[34]

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#.

48 SubSNP, 40 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95700085	Oct 12, 2018 (152)
2	SSMP	ss664373811	Apr 01, 2015 (144)
3	EVA_UK10K_ALSPAC	ss1708836736	Apr 01, 2015 (144)
4	EVA_UK10K_TWINSUK	ss1708836929	Apr 01, 2015 (144)
5	SWEGEN	ss3015851344	Nov 08, 2017 (151)
6	SWEGEN	ss3015851345	Nov 08, 2017 (151)
7	SWEGEN	ss3015851346	Nov 08, 2017 (151)
8	MCHAISSO	ss3065661304	Jan 10, 2018 (151)
9	ACPOP	ss3742188298	Jul 13, 2019 (153)
10	ACPOP	ss3742188299	Jul 13, 2019 (153)
11	ACPOP	ss3742188303	Jul 13, 2019 (153)
12	EVA	ss3834961362	Apr 27, 2020 (154)
13	KOGIC	ss3979226962	Apr 27, 2020 (154)
14	KOGIC	ss3979226963	Apr 27, 2020 (154)
15	KOGIC	ss3979226966	Apr 27, 2020 (154)
16	GNOMAD	ss4315136098	Apr 26, 2021 (155)
17	GNOMAD	ss4315136099	Apr 26, 2021 (155)
18	GNOMAD	ss4315136100	Apr 26, 2021 (155)
19	GNOMAD	ss4315136135	Apr 26, 2021 (155)
20	GNOMAD	ss4315136136	Apr 26, 2021 (155)
21	GNOMAD	ss4315136137	Apr 26, 2021 (155)
22	GNOMAD	ss4315136138	Apr 26, 2021 (155)
23	GNOMAD	ss4315136139	Apr 26, 2021 (155)
24	GNOMAD	ss4315136140	Apr 26, 2021 (155)
25	GNOMAD	ss4315136141	Apr 26, 2021 (155)
26	GNOMAD	ss4315136142	Apr 26, 2021 (155)
27	GNOMAD	ss4315136143	Apr 26, 2021 (155)
28	GNOMAD	ss4315136144	Apr 26, 2021 (155)
29	GNOMAD	ss4315136145	Apr 26, 2021 (155)
30	GNOMAD	ss4315136146	Apr 26, 2021 (155)
31	GNOMAD	ss4315136147	Apr 26, 2021 (155)
32	GNOMAD	ss4315136148	Apr 26, 2021 (155)
33	GNOMAD	ss4315136149	Apr 26, 2021 (155)
34	GNOMAD	ss4315136150	Apr 26, 2021 (155)
35	GNOMAD	ss4315136151	Apr 26, 2021 (155)
36	GNOMAD	ss4315136152	Apr 26, 2021 (155)
37	GNOMAD	ss4315136153	Apr 26, 2021 (155)
38	GNOMAD	ss4315136154	Apr 26, 2021 (155)
39	GNOMAD	ss4315136155	Apr 26, 2021 (155)
40	TOPMED	ss5042796152	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5223330879	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5223330881	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5223330883	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5779830690	Oct 16, 2022 (156)
45	TOMMO_GENOMICS	ss5779830691	Oct 16, 2022 (156)
46	TOMMO_GENOMICS	ss5779830694	Oct 16, 2022 (156)
47	EVA	ss5834243255	Oct 16, 2022 (156)
48	EVA	ss5834243256	Oct 16, 2022 (156)
49	The Avon Longitudinal Study of Parents and Children	NC_000017.10 - 69118970	Oct 12, 2018 (152)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512987031 (NC_000017.11:71122828::AG 2247/84726) Row 512987032 (NC_000017.11:71122828::AGAG 14844/83852) Row 512987033 (NC_000017.11:71122828::AGAGAG 4191/84520)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512987031 (NC_000017.11:71122828::AG 2247/84726) Row 512987032 (NC_000017.11:71122828::AGAG 14844/83852) Row 512987033 (NC_000017.11:71122828::AGAGAG 4191/84520)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512987031 (NC_000017.11:71122828::AG 2247/84726) Row 512987032 (NC_000017.11:71122828::AGAG 14844/83852) Row 512987033 (NC_000017.11:71122828::AGAGAG 4191/84520)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512987031 (NC_000017.11:71122828::AG 2247/84726) Row 512987032 (NC_000017.11:71122828::AGAG 14844/83852) Row 512987033 (NC_000017.11:71122828::AGAGAG 4191/84520)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512987031 (NC_000017.11:71122828::AG 2247/84726) Row 512987032 (NC_000017.11:71122828::AGAG 14844/83852) Row 512987033 (NC_000017.11:71122828::AGAGAG 4191/84520)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512987031 (NC_000017.11:71122828::AG 2247/84726) Row 512987032 (NC_000017.11:71122828::AGAG 14844/83852) Row 512987033 (NC_000017.11:71122828::AGAGAG 4191/84520)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512987031 (NC_000017.11:71122828::AG 2247/84726) Row 512987032 (NC_000017.11:71122828::AGAG 14844/83852) Row 512987033 (NC_000017.11:71122828::AGAGAG 4191/84520)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512987031 (NC_000017.11:71122828::AG 2247/84726) Row 512987032 (NC_000017.11:71122828::AGAG 14844/83852) Row 512987033 (NC_000017.11:71122828::AGAGAG 4191/84520)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512987031 (NC_000017.11:71122828::AG 2247/84726) Row 512987032 (NC_000017.11:71122828::AGAG 14844/83852) Row 512987033 (NC_000017.11:71122828::AGAGAG 4191/84520)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512987031 (NC_000017.11:71122828::AG 2247/84726) Row 512987032 (NC_000017.11:71122828::AGAG 14844/83852) Row 512987033 (NC_000017.11:71122828::AGAGAG 4191/84520)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512987031 (NC_000017.11:71122828::AG 2247/84726) Row 512987032 (NC_000017.11:71122828::AGAG 14844/83852) Row 512987033 (NC_000017.11:71122828::AGAGAG 4191/84520)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512987031 (NC_000017.11:71122828::AG 2247/84726) Row 512987032 (NC_000017.11:71122828::AGAG 14844/83852) Row 512987033 (NC_000017.11:71122828::AGAGAG 4191/84520)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512987031 (NC_000017.11:71122828::AG 2247/84726) Row 512987032 (NC_000017.11:71122828::AGAG 14844/83852) Row 512987033 (NC_000017.11:71122828::AGAGAG 4191/84520)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512987031 (NC_000017.11:71122828::AG 2247/84726) Row 512987032 (NC_000017.11:71122828::AGAG 14844/83852) Row 512987033 (NC_000017.11:71122828::AGAGAG 4191/84520)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512987031 (NC_000017.11:71122828::AG 2247/84726) Row 512987032 (NC_000017.11:71122828::AGAG 14844/83852) Row 512987033 (NC_000017.11:71122828::AGAGAG 4191/84520)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512987031 (NC_000017.11:71122828::AG 2247/84726) Row 512987032 (NC_000017.11:71122828::AGAG 14844/83852) Row 512987033 (NC_000017.11:71122828::AGAGAG 4191/84520)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512987031 (NC_000017.11:71122828::AG 2247/84726) Row 512987032 (NC_000017.11:71122828::AGAG 14844/83852) Row 512987033 (NC_000017.11:71122828::AGAGAG 4191/84520)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512987031 (NC_000017.11:71122828::AG 2247/84726) Row 512987032 (NC_000017.11:71122828::AGAG 14844/83852) Row 512987033 (NC_000017.11:71122828::AGAGAG 4191/84520)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512987031 (NC_000017.11:71122828::AG 2247/84726) Row 512987032 (NC_000017.11:71122828::AGAG 14844/83852) Row 512987033 (NC_000017.11:71122828::AGAGAG 4191/84520)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512987031 (NC_000017.11:71122828::AG 2247/84726) Row 512987032 (NC_000017.11:71122828::AGAG 14844/83852) Row 512987033 (NC_000017.11:71122828::AGAGAG 4191/84520)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512987031 (NC_000017.11:71122828::AG 2247/84726) Row 512987032 (NC_000017.11:71122828::AGAG 14844/83852) Row 512987033 (NC_000017.11:71122828::AGAGAG 4191/84520)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512987031 (NC_000017.11:71122828::AG 2247/84726) Row 512987032 (NC_000017.11:71122828::AGAG 14844/83852) Row 512987033 (NC_000017.11:71122828::AGAGAG 4191/84520)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512987031 (NC_000017.11:71122828::AG 2247/84726) Row 512987032 (NC_000017.11:71122828::AGAG 14844/83852) Row 512987033 (NC_000017.11:71122828::AGAGAG 4191/84520)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 512987031 (NC_000017.11:71122828::AG 2247/84726) Row 512987032 (NC_000017.11:71122828::AGAG 14844/83852) Row 512987033 (NC_000017.11:71122828::AGAGAG 4191/84520)...	-	Apr 26, 2021 (155)
74	Korean Genome Project Submission ignored due to conflicting rows: Row 35604963 (NC_000017.11:71122828::AG 203/1724) Row 35604964 (NC_000017.11:71122828::AGAG 134/1724) Row 35604967 (NC_000017.11:71122828::AGAGAG 63/1724)	-	Apr 27, 2020 (154)
75	Korean Genome Project Submission ignored due to conflicting rows: Row 35604963 (NC_000017.11:71122828::AG 203/1724) Row 35604964 (NC_000017.11:71122828::AGAG 134/1724) Row 35604967 (NC_000017.11:71122828::AGAGAG 63/1724)	-	Apr 27, 2020 (154)
76	Korean Genome Project Submission ignored due to conflicting rows: Row 35604963 (NC_000017.11:71122828::AG 203/1724) Row 35604964 (NC_000017.11:71122828::AGAG 134/1724) Row 35604967 (NC_000017.11:71122828::AGAGAG 63/1724)	-	Apr 27, 2020 (154)
77	Northern Sweden Submission ignored due to conflicting rows: Row 15473163 (NC_000017.10:69118969::AG 48/582) Row 15473164 (NC_000017.10:69118969::AGAG 113/582) Row 15473168 (NC_000017.10:69118969::AGAGAG 14/582)	-	Jul 13, 2019 (153)
78	Northern Sweden Submission ignored due to conflicting rows: Row 15473163 (NC_000017.10:69118969::AG 48/582) Row 15473164 (NC_000017.10:69118969::AGAG 113/582) Row 15473168 (NC_000017.10:69118969::AGAGAG 14/582)	-	Jul 13, 2019 (153)
79	Northern Sweden Submission ignored due to conflicting rows: Row 15473163 (NC_000017.10:69118969::AG 48/582) Row 15473164 (NC_000017.10:69118969::AGAG 113/582) Row 15473168 (NC_000017.10:69118969::AGAGAG 14/582)	-	Jul 13, 2019 (153)
80	8.3KJPN Submission ignored due to conflicting rows: Row 81300186 (NC_000017.10:69118969::AGAG 1619/14678) Row 81300188 (NC_000017.10:69118969::AG 1525/14678) Row 81300190 (NC_000017.10:69118969::AGAGAG 422/14678)	-	Apr 26, 2021 (155)
81	8.3KJPN Submission ignored due to conflicting rows: Row 81300186 (NC_000017.10:69118969::AGAG 1619/14678) Row 81300188 (NC_000017.10:69118969::AG 1525/14678) Row 81300190 (NC_000017.10:69118969::AGAGAG 422/14678)	-	Apr 26, 2021 (155)
82	8.3KJPN Submission ignored due to conflicting rows: Row 81300186 (NC_000017.10:69118969::AGAG 1619/14678) Row 81300188 (NC_000017.10:69118969::AG 1525/14678) Row 81300190 (NC_000017.10:69118969::AGAGAG 422/14678)	-	Apr 26, 2021 (155)
83	14KJPN Submission ignored due to conflicting rows: Row 113667794 (NC_000017.11:71122828::AGAGAG 686/28172) Row 113667795 (NC_000017.11:71122828::AGAG 2583/28172) Row 113667798 (NC_000017.11:71122828::AG 2531/28172)	-	Oct 16, 2022 (156)
84	14KJPN Submission ignored due to conflicting rows: Row 113667794 (NC_000017.11:71122828::AGAGAG 686/28172) Row 113667795 (NC_000017.11:71122828::AGAG 2583/28172) Row 113667798 (NC_000017.11:71122828::AG 2531/28172)	-	Oct 16, 2022 (156)
85	14KJPN Submission ignored due to conflicting rows: Row 113667794 (NC_000017.11:71122828::AGAGAG 686/28172) Row 113667795 (NC_000017.11:71122828::AGAG 2583/28172) Row 113667798 (NC_000017.11:71122828::AG 2531/28172)	-	Oct 16, 2022 (156)
86	TopMed	NC_000017.11 - 71122829	Apr 26, 2021 (155)
87	UK 10K study - Twins	NC_000017.10 - 69118970	Oct 12, 2018 (152)
88	ALFA	NC_000017.11 - 71122829	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
ss4315136155	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAG:	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGA	(self)
2980734582	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGA	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGA	(self)
ss4315136154	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAG:	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGA	(self)
2980734582	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGA	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4315136153	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAG:	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGA	(self)
2980734582	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGA	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGA	(self)
258341814, ss4315136152, ss5042796152	NC_000017.11:71122828:AGAGAGAGAGAG:	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
2980734582	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4315136151	NC_000017.11:71122828:AGAGAGAGAG:	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
2980734582	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4315136150	NC_000017.11:71122828:AGAGAGAG:	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
2980734582	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4315136149	NC_000017.11:71122828:AGAGAG:	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
2980734582	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4315136148	NC_000017.11:71122828:AGAG:	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
2980734582	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss3065661304, ss4315136147	NC_000017.11:71122828:AG:	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
2980734582	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss3015851345, ss3742188298, ss5223330881	NC_000017.10:69118969::AG	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss3979226962, ss4315136098, ss5779830694	NC_000017.11:71122828::AG	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
2980734582	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
40279442, 40279442, ss664373811, ss1708836736, ss1708836929, ss3015851344, ss3742188299, ss3834961362, ss5223330879, ss5834243255	NC_000017.10:69118969::AGAG	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss3979226963, ss4315136099, ss5779830691	NC_000017.11:71122828::AGAG	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
2980734582	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss95700085	NT_010783.15:34393160::GAGA	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss3015851346, ss3742188303, ss5223330883, ss5834243256	NC_000017.10:69118969::AGAGAG	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss3979226966, ss4315136100, ss5779830690	NC_000017.11:71122828::AGAGAG	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
2980734582	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4315136135	NC_000017.11:71122828::AGAGAGAG	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
2980734582	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4315136136	NC_000017.11:71122828::AGAGAGAGAG	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
2980734582	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4315136137	NC_000017.11:71122828::AGAGAGAGAGAG	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
2980734582	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4315136138	NC_000017.11:71122828::AGAGAGAGAGA… NC_000017.11:71122828::AGAGAGAGAGAGAG	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
2980734582	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4315136139	NC_000017.11:71122828::AGAGAGAGAGA… NC_000017.11:71122828::AGAGAGAGAGAGAGAG	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4315136140	NC_000017.11:71122828::AGAGAGAGAGA… NC_000017.11:71122828::AGAGAGAGAGAGAGAGAG	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4315136141	NC_000017.11:71122828::AGAGAGAGAGA… NC_000017.11:71122828::AGAGAGAGAGAGAGAGAGAG	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4315136142	NC_000017.11:71122828::AGAGAGAGAGA… NC_000017.11:71122828::AGAGAGAGAGAGAGAGAGAGAG	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4315136143	NC_000017.11:71122828::AGAGAGAGAGA… NC_000017.11:71122828::AGAGAGAGAGAGAGAGAGAGAGAG	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4315136144	NC_000017.11:71122828::AGAGAGAGAGA… NC_000017.11:71122828::AGAGAGAGAGAGAGAGAGAGAGAGAG	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4315136145	NC_000017.11:71122828::AGAGAGAGAGA… NC_000017.11:71122828::AGAGAGAGAGAGAGAGAGAGAGAGAGAG	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4315136146	NC_000017.11:71122828::AGAGAGAGAGA… NC_000017.11:71122828::AGAGAGAGAGAGAGAGAGAGAGAGAGAGAG	NC_000017.11:71122828:AGAGAGAGAGAG… NC_000017.11:71122828:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(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 rs778856865

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

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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

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Reference SNP (rs) Report

rs778856865