Name: rs34972570
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.

rs34972570

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr19:3972315-3972339 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₁₇ / del(T)₁₄ / del(T)₁₃ / d…
del(T)₁₇ / del(T)₁₄ / del(T)₁₃ / del(T)₁₂ / del(T)₁₁ / del(T)₁₀ / del(T)₉ / del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₀ / dup(T)₁₁ / dup(T)₁₂ / dup(T)₁₃ / dup(T)₁₄ / dup(T)₁₅
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.2867 (1539/5368, ALFA)
(T)₂₅=0.0158 (61/3854, ALSPAC)
(T)₂₅=0.0194 (72/3708, TWINSUK) (+ 1 more)
(T)₂₅=0.28 (11/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: DAPK3 : 2KB Upstream Variant
Publications: 0 citations
Genomic View: See rs on genome

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

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	5368	TTTTTTTTTTTTTTTTTTTTTTTTT=0.5894	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0030, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.2867, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0971, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0041, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0179, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0019, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.682825	0.252078	0.065097	32
European	Sub	4942	TTTTTTTTTTTTTTTTTTTTTTTTT=0.5552	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0032, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.3104, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.1054, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0045, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0192, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0020, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.649437	0.278403	0.07216	32
African	Sub	358	TTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	12	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	346	TTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	4	TTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	4	TTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	4	TTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	16	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	2	TTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other	Sub	42	TTTTTTTTTTTTTTTTTTTTTTTTT=0.86	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.12, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.02, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	0.9	0.1	0.0	11

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

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	5368	(T)₂₅=0.5894	del(T)₁₄=0.0000, del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0030, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.2867, dupTT=0.0971, dupTTT=0.0179, dup(T)₄=0.0041, dup(T)₆=0.0019, dup(T)₇=0.0000
Allele Frequency Aggregator	European	Sub	4942	(T)₂₅=0.5552	del(T)₁₄=0.0000, del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0032, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.3104, dupTT=0.1054, dupTTT=0.0192, dup(T)₄=0.0045, dup(T)₆=0.0020, dup(T)₇=0.0000
Allele Frequency Aggregator	African	Sub	358	(T)₂₅=1.000	del(T)₁₄=0.000, del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₆=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	Other	Sub	42	(T)₂₅=0.86	del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.12, dupTT=0.00, dupTTT=0.02, dup(T)₄=0.00, dup(T)₆=0.00, dup(T)₇=0.00
Allele Frequency Aggregator	Latin American 2	Sub	16	(T)₂₅=1.00	del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₆=0.00, dup(T)₇=0.00
Allele Frequency Aggregator	Latin American 1	Sub	4	(T)₂₅=1.0	del(T)₁₄=0.0, del(T)₁₃=0.0, del(T)₁₂=0.0, del(T)₁₁=0.0, del(T)₁₀=0.0, del(T)₉=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₆=0.0, dup(T)₇=0.0
Allele Frequency Aggregator	Asian	Sub	4	(T)₂₅=1.0	del(T)₁₄=0.0, del(T)₁₃=0.0, del(T)₁₂=0.0, del(T)₁₁=0.0, del(T)₁₀=0.0, del(T)₉=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₆=0.0, dup(T)₇=0.0
Allele Frequency Aggregator	South Asian	Sub	2	(T)₂₅=1.0	del(T)₁₄=0.0, del(T)₁₃=0.0, del(T)₁₂=0.0, del(T)₁₁=0.0, del(T)₁₀=0.0, del(T)₉=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₆=0.0, dup(T)₇=0.0
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	- No frequency provided	dupT=0.9842
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	- No frequency provided	dupT=0.9806
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupT=0.72

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.3972323_3972339del
GRCh38.p14 chr 19	NC_000019.10:g.3972326_3972339del
GRCh38.p14 chr 19	NC_000019.10:g.3972327_3972339del
GRCh38.p14 chr 19	NC_000019.10:g.3972328_3972339del
GRCh38.p14 chr 19	NC_000019.10:g.3972329_3972339del
GRCh38.p14 chr 19	NC_000019.10:g.3972330_3972339del
GRCh38.p14 chr 19	NC_000019.10:g.3972331_3972339del
GRCh38.p14 chr 19	NC_000019.10:g.3972332_3972339del
GRCh38.p14 chr 19	NC_000019.10:g.3972333_3972339del
GRCh38.p14 chr 19	NC_000019.10:g.3972334_3972339del
GRCh38.p14 chr 19	NC_000019.10:g.3972335_3972339del
GRCh38.p14 chr 19	NC_000019.10:g.3972336_3972339del
GRCh38.p14 chr 19	NC_000019.10:g.3972337_3972339del
GRCh38.p14 chr 19	NC_000019.10:g.3972338_3972339del
GRCh38.p14 chr 19	NC_000019.10:g.3972339del
GRCh38.p14 chr 19	NC_000019.10:g.3972339dup
GRCh38.p14 chr 19	NC_000019.10:g.3972338_3972339dup
GRCh38.p14 chr 19	NC_000019.10:g.3972337_3972339dup
GRCh38.p14 chr 19	NC_000019.10:g.3972336_3972339dup
GRCh38.p14 chr 19	NC_000019.10:g.3972335_3972339dup
GRCh38.p14 chr 19	NC_000019.10:g.3972334_3972339dup
GRCh38.p14 chr 19	NC_000019.10:g.3972333_3972339dup
GRCh38.p14 chr 19	NC_000019.10:g.3972332_3972339dup
GRCh38.p14 chr 19	NC_000019.10:g.3972331_3972339dup
GRCh38.p14 chr 19	NC_000019.10:g.3972330_3972339dup
GRCh38.p14 chr 19	NC_000019.10:g.3972329_3972339dup
GRCh38.p14 chr 19	NC_000019.10:g.3972328_3972339dup
GRCh38.p14 chr 19	NC_000019.10:g.3972327_3972339dup
GRCh38.p14 chr 19	NC_000019.10:g.3972326_3972339dup
GRCh38.p14 chr 19	NC_000019.10:g.3972325_3972339dup
GRCh37.p13 chr 19	NC_000019.9:g.3972321_3972337del
GRCh37.p13 chr 19	NC_000019.9:g.3972324_3972337del
GRCh37.p13 chr 19	NC_000019.9:g.3972325_3972337del
GRCh37.p13 chr 19	NC_000019.9:g.3972326_3972337del
GRCh37.p13 chr 19	NC_000019.9:g.3972327_3972337del
GRCh37.p13 chr 19	NC_000019.9:g.3972328_3972337del
GRCh37.p13 chr 19	NC_000019.9:g.3972329_3972337del
GRCh37.p13 chr 19	NC_000019.9:g.3972330_3972337del
GRCh37.p13 chr 19	NC_000019.9:g.3972331_3972337del
GRCh37.p13 chr 19	NC_000019.9:g.3972332_3972337del
GRCh37.p13 chr 19	NC_000019.9:g.3972333_3972337del
GRCh37.p13 chr 19	NC_000019.9:g.3972334_3972337del
GRCh37.p13 chr 19	NC_000019.9:g.3972335_3972337del
GRCh37.p13 chr 19	NC_000019.9:g.3972336_3972337del
GRCh37.p13 chr 19	NC_000019.9:g.3972337del
GRCh37.p13 chr 19	NC_000019.9:g.3972337dup
GRCh37.p13 chr 19	NC_000019.9:g.3972336_3972337dup
GRCh37.p13 chr 19	NC_000019.9:g.3972335_3972337dup
GRCh37.p13 chr 19	NC_000019.9:g.3972334_3972337dup
GRCh37.p13 chr 19	NC_000019.9:g.3972333_3972337dup
GRCh37.p13 chr 19	NC_000019.9:g.3972332_3972337dup
GRCh37.p13 chr 19	NC_000019.9:g.3972331_3972337dup
GRCh37.p13 chr 19	NC_000019.9:g.3972330_3972337dup
GRCh37.p13 chr 19	NC_000019.9:g.3972329_3972337dup
GRCh37.p13 chr 19	NC_000019.9:g.3972328_3972337dup
GRCh37.p13 chr 19	NC_000019.9:g.3972327_3972337dup
GRCh37.p13 chr 19	NC_000019.9:g.3972326_3972337dup
GRCh37.p13 chr 19	NC_000019.9:g.3972325_3972337dup
GRCh37.p13 chr 19	NC_000019.9:g.3972324_3972337dup
GRCh37.p13 chr 19	NC_000019.9:g.3972323_3972337dup

Gene: DAPK3, death associated protein kinase 3 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
DAPK3 transcript variant 1	NM_001348.3:c.	N/A	Upstream Transcript Variant
DAPK3 transcript variant 2	NM_001375658.1: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	(T)₂₅=	del(T)₁₇	del(T)₁₄	del(T)₁₃	del(T)₁₂	del(T)₁₁	del(T)₁₀	del(T)₉	del(T)₈	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₀	dup(T)₁₁	dup(T)₁₂	dup(T)₁₃	dup(T)₁₄	dup(T)₁₅
GRCh38.p14 chr 19	NC_000019.10:g.3972315_3972339=	NC_000019.10:g.3972323_3972339del	NC_000019.10:g.3972326_3972339del	NC_000019.10:g.3972327_3972339del	NC_000019.10:g.3972328_3972339del	NC_000019.10:g.3972329_3972339del	NC_000019.10:g.3972330_3972339del	NC_000019.10:g.3972331_3972339del	NC_000019.10:g.3972332_3972339del	NC_000019.10:g.3972333_3972339del	NC_000019.10:g.3972334_3972339del	NC_000019.10:g.3972335_3972339del	NC_000019.10:g.3972336_3972339del	NC_000019.10:g.3972337_3972339del	NC_000019.10:g.3972338_3972339del	NC_000019.10:g.3972339del	NC_000019.10:g.3972339dup	NC_000019.10:g.3972338_3972339dup	NC_000019.10:g.3972337_3972339dup	NC_000019.10:g.3972336_3972339dup	NC_000019.10:g.3972335_3972339dup	NC_000019.10:g.3972334_3972339dup	NC_000019.10:g.3972333_3972339dup	NC_000019.10:g.3972332_3972339dup	NC_000019.10:g.3972331_3972339dup	NC_000019.10:g.3972330_3972339dup	NC_000019.10:g.3972329_3972339dup	NC_000019.10:g.3972328_3972339dup	NC_000019.10:g.3972327_3972339dup	NC_000019.10:g.3972326_3972339dup	NC_000019.10:g.3972325_3972339dup
GRCh37.p13 chr 19	NC_000019.9:g.3972313_3972337=	NC_000019.9:g.3972321_3972337del	NC_000019.9:g.3972324_3972337del	NC_000019.9:g.3972325_3972337del	NC_000019.9:g.3972326_3972337del	NC_000019.9:g.3972327_3972337del	NC_000019.9:g.3972328_3972337del	NC_000019.9:g.3972329_3972337del	NC_000019.9:g.3972330_3972337del	NC_000019.9:g.3972331_3972337del	NC_000019.9:g.3972332_3972337del	NC_000019.9:g.3972333_3972337del	NC_000019.9:g.3972334_3972337del	NC_000019.9:g.3972335_3972337del	NC_000019.9:g.3972336_3972337del	NC_000019.9:g.3972337del	NC_000019.9:g.3972337dup	NC_000019.9:g.3972336_3972337dup	NC_000019.9:g.3972335_3972337dup	NC_000019.9:g.3972334_3972337dup	NC_000019.9:g.3972333_3972337dup	NC_000019.9:g.3972332_3972337dup	NC_000019.9:g.3972331_3972337dup	NC_000019.9:g.3972330_3972337dup	NC_000019.9:g.3972329_3972337dup	NC_000019.9:g.3972328_3972337dup	NC_000019.9:g.3972327_3972337dup	NC_000019.9:g.3972326_3972337dup	NC_000019.9:g.3972325_3972337dup	NC_000019.9:g.3972324_3972337dup	NC_000019.9:g.3972323_3972337dup

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#.

57 SubSNP, 53 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41027229	Mar 14, 2006 (126)
2	PJP	ss294951674	May 09, 2011 (138)
3	SSMP	ss664442695	Apr 01, 2015 (144)
4	EVA_GENOME_DK	ss1575221902	Apr 01, 2015 (144)
5	EVA_UK10K_ALSPAC	ss1709098601	Apr 01, 2015 (144)
6	EVA_UK10K_TWINSUK	ss1709098610	Apr 01, 2015 (144)
7	EVA_EXAC	ss1712178570	Apr 01, 2015 (144)
8	EVA_EXAC	ss1712178571	Apr 01, 2015 (144)
9	EVA_EXAC	ss1712178572	Apr 01, 2015 (144)
10	EVA_EXAC	ss1712178573	Apr 01, 2015 (144)
11	EVA_EXAC	ss1712178574	Apr 01, 2015 (144)
12	SWEGEN	ss3016997959	Nov 08, 2017 (151)
13	FSA-LAB	ss3984139409	Apr 26, 2021 (155)
14	GNOMAD	ss4326724643	Apr 26, 2021 (155)
15	GNOMAD	ss4326724644	Apr 26, 2021 (155)
16	GNOMAD	ss4326724645	Apr 26, 2021 (155)
17	GNOMAD	ss4326724646	Apr 26, 2021 (155)
18	GNOMAD	ss4326724647	Apr 26, 2021 (155)
19	GNOMAD	ss4326724648	Apr 26, 2021 (155)
20	GNOMAD	ss4326724649	Apr 26, 2021 (155)
21	GNOMAD	ss4326724650	Apr 26, 2021 (155)
22	GNOMAD	ss4326724651	Apr 26, 2021 (155)
23	GNOMAD	ss4326724652	Apr 26, 2021 (155)
24	GNOMAD	ss4326724653	Apr 26, 2021 (155)
25	GNOMAD	ss4326724654	Apr 26, 2021 (155)
26	GNOMAD	ss4326724655	Apr 26, 2021 (155)
27	GNOMAD	ss4326724657	Apr 26, 2021 (155)
28	GNOMAD	ss4326724658	Apr 26, 2021 (155)
29	GNOMAD	ss4326724659	Apr 26, 2021 (155)
30	GNOMAD	ss4326724660	Apr 26, 2021 (155)
31	GNOMAD	ss4326724661	Apr 26, 2021 (155)
32	GNOMAD	ss4326724662	Apr 26, 2021 (155)
33	GNOMAD	ss4326724663	Apr 26, 2021 (155)
34	GNOMAD	ss4326724664	Apr 26, 2021 (155)
35	GNOMAD	ss4326724665	Apr 26, 2021 (155)
36	GNOMAD	ss4326724666	Apr 26, 2021 (155)
37	GNOMAD	ss4326724667	Apr 26, 2021 (155)
38	GNOMAD	ss4326724668	Apr 26, 2021 (155)
39	GNOMAD	ss4326724669	Apr 26, 2021 (155)
40	GNOMAD	ss4326724670	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5226464694	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5226464695	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5226464696	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5226464697	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5226464698	Apr 26, 2021 (155)
46	1000G_HIGH_COVERAGE	ss5306291109	Oct 16, 2022 (156)
47	1000G_HIGH_COVERAGE	ss5306291110	Oct 16, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5306291111	Oct 16, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5306291112	Oct 16, 2022 (156)
50	TOMMO_GENOMICS	ss5784648086	Oct 16, 2022 (156)
51	TOMMO_GENOMICS	ss5784648087	Oct 16, 2022 (156)
52	TOMMO_GENOMICS	ss5784648088	Oct 16, 2022 (156)
53	TOMMO_GENOMICS	ss5784648089	Oct 16, 2022 (156)
54	TOMMO_GENOMICS	ss5784648090	Oct 16, 2022 (156)
55	EVA	ss5840177334	Oct 16, 2022 (156)
56	EVA	ss5840177335	Oct 16, 2022 (156)
57	EVA	ss5953294781	Oct 16, 2022 (156)
58	The Avon Longitudinal Study of Parents and Children	NC_000019.9 - 3972313	Oct 12, 2018 (152)
59	ExAC Submission ignored due to conflicting rows: Row 3749466 (NC_000019.9:3972312::T 0/596) Row 3749467 (NC_000019.9:3972312::TT 0/596) Row 3749468 (NC_000019.9:3972312::TTT 0/596) Row 3749469 (NC_000019.9:3972312::TTTT 2/596) Row 3749470 (NC_000019.9:3972312::TTTTT 0/596)	-	Oct 12, 2018 (152)
60	ExAC Submission ignored due to conflicting rows: Row 3749466 (NC_000019.9:3972312::T 0/596) Row 3749467 (NC_000019.9:3972312::TT 0/596) Row 3749468 (NC_000019.9:3972312::TTT 0/596) Row 3749469 (NC_000019.9:3972312::TTTT 2/596) Row 3749470 (NC_000019.9:3972312::TTTTT 0/596)	-	Oct 12, 2018 (152)
61	ExAC Submission ignored due to conflicting rows: Row 3749466 (NC_000019.9:3972312::T 0/596) Row 3749467 (NC_000019.9:3972312::TT 0/596) Row 3749468 (NC_000019.9:3972312::TTT 0/596) Row 3749469 (NC_000019.9:3972312::TTTT 2/596) Row 3749470 (NC_000019.9:3972312::TTTTT 0/596)	-	Oct 12, 2018 (152)
62	ExAC Submission ignored due to conflicting rows: Row 3749466 (NC_000019.9:3972312::T 0/596) Row 3749467 (NC_000019.9:3972312::TT 0/596) Row 3749468 (NC_000019.9:3972312::TTT 0/596) Row 3749469 (NC_000019.9:3972312::TTTT 2/596) Row 3749470 (NC_000019.9:3972312::TTTTT 0/596)	-	Oct 12, 2018 (152)
63	ExAC Submission ignored due to conflicting rows: Row 3749466 (NC_000019.9:3972312::T 0/596) Row 3749467 (NC_000019.9:3972312::TT 0/596) Row 3749468 (NC_000019.9:3972312::TTT 0/596) Row 3749469 (NC_000019.9:3972312::TTTT 2/596) Row 3749470 (NC_000019.9:3972312::TTTTT 0/596)	-	Oct 12, 2018 (152)
64	The Danish reference pan genome	NC_000019.9 - 3972313	Apr 27, 2020 (154)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532526174 (NC_000019.10:3972314::T 35278/58354) Row 532526175 (NC_000019.10:3972314::TTTT 285/58160) Row 532526176 (NC_000019.10:3972314::TTTTT 71/58172)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532526174 (NC_000019.10:3972314::T 35278/58354) Row 532526175 (NC_000019.10:3972314::TTTT 285/58160) Row 532526176 (NC_000019.10:3972314::TTTTT 71/58172)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532526174 (NC_000019.10:3972314::T 35278/58354) Row 532526175 (NC_000019.10:3972314::TTTT 285/58160) Row 532526176 (NC_000019.10:3972314::TTTTT 71/58172)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532526174 (NC_000019.10:3972314::T 35278/58354) Row 532526175 (NC_000019.10:3972314::TTTT 285/58160) Row 532526176 (NC_000019.10:3972314::TTTTT 71/58172)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532526174 (NC_000019.10:3972314::T 35278/58354) Row 532526175 (NC_000019.10:3972314::TTTT 285/58160) Row 532526176 (NC_000019.10:3972314::TTTTT 71/58172)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532526174 (NC_000019.10:3972314::T 35278/58354) Row 532526175 (NC_000019.10:3972314::TTTT 285/58160) Row 532526176 (NC_000019.10:3972314::TTTTT 71/58172)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532526174 (NC_000019.10:3972314::T 35278/58354) Row 532526175 (NC_000019.10:3972314::TTTT 285/58160) Row 532526176 (NC_000019.10:3972314::TTTTT 71/58172)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532526174 (NC_000019.10:3972314::T 35278/58354) Row 532526175 (NC_000019.10:3972314::TTTT 285/58160) Row 532526176 (NC_000019.10:3972314::TTTTT 71/58172)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532526174 (NC_000019.10:3972314::T 35278/58354) Row 532526175 (NC_000019.10:3972314::TTTT 285/58160) Row 532526176 (NC_000019.10:3972314::TTTTT 71/58172)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532526174 (NC_000019.10:3972314::T 35278/58354) Row 532526175 (NC_000019.10:3972314::TTTT 285/58160) Row 532526176 (NC_000019.10:3972314::TTTTT 71/58172)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532526174 (NC_000019.10:3972314::T 35278/58354) Row 532526175 (NC_000019.10:3972314::TTTT 285/58160) Row 532526176 (NC_000019.10:3972314::TTTTT 71/58172)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532526174 (NC_000019.10:3972314::T 35278/58354) Row 532526175 (NC_000019.10:3972314::TTTT 285/58160) Row 532526176 (NC_000019.10:3972314::TTTTT 71/58172)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532526174 (NC_000019.10:3972314::T 35278/58354) Row 532526175 (NC_000019.10:3972314::TTTT 285/58160) Row 532526176 (NC_000019.10:3972314::TTTTT 71/58172)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532526174 (NC_000019.10:3972314::T 35278/58354) Row 532526175 (NC_000019.10:3972314::TTTT 285/58160) Row 532526176 (NC_000019.10:3972314::TTTTT 71/58172)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532526174 (NC_000019.10:3972314::T 35278/58354) Row 532526175 (NC_000019.10:3972314::TTTT 285/58160) Row 532526176 (NC_000019.10:3972314::TTTTT 71/58172)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532526174 (NC_000019.10:3972314::T 35278/58354) Row 532526175 (NC_000019.10:3972314::TTTT 285/58160) Row 532526176 (NC_000019.10:3972314::TTTTT 71/58172)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532526174 (NC_000019.10:3972314::T 35278/58354) Row 532526175 (NC_000019.10:3972314::TTTT 285/58160) Row 532526176 (NC_000019.10:3972314::TTTTT 71/58172)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532526174 (NC_000019.10:3972314::T 35278/58354) Row 532526175 (NC_000019.10:3972314::TTTT 285/58160) Row 532526176 (NC_000019.10:3972314::TTTTT 71/58172)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532526174 (NC_000019.10:3972314::T 35278/58354) Row 532526175 (NC_000019.10:3972314::TTTT 285/58160) Row 532526176 (NC_000019.10:3972314::TTTTT 71/58172)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532526174 (NC_000019.10:3972314::T 35278/58354) Row 532526175 (NC_000019.10:3972314::TTTT 285/58160) Row 532526176 (NC_000019.10:3972314::TTTTT 71/58172)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532526174 (NC_000019.10:3972314::T 35278/58354) Row 532526175 (NC_000019.10:3972314::TTTT 285/58160) Row 532526176 (NC_000019.10:3972314::TTTTT 71/58172)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532526174 (NC_000019.10:3972314::T 35278/58354) Row 532526175 (NC_000019.10:3972314::TTTT 285/58160) Row 532526176 (NC_000019.10:3972314::TTTTT 71/58172)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532526174 (NC_000019.10:3972314::T 35278/58354) Row 532526175 (NC_000019.10:3972314::TTTT 285/58160) Row 532526176 (NC_000019.10:3972314::TTTTT 71/58172)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532526174 (NC_000019.10:3972314::T 35278/58354) Row 532526175 (NC_000019.10:3972314::TTTT 285/58160) Row 532526176 (NC_000019.10:3972314::TTTTT 71/58172)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532526174 (NC_000019.10:3972314::T 35278/58354) Row 532526175 (NC_000019.10:3972314::TTTT 285/58160) Row 532526176 (NC_000019.10:3972314::TTTTT 71/58172)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532526174 (NC_000019.10:3972314::T 35278/58354) Row 532526175 (NC_000019.10:3972314::TTTT 285/58160) Row 532526176 (NC_000019.10:3972314::TTTTT 71/58172)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532526174 (NC_000019.10:3972314::T 35278/58354) Row 532526175 (NC_000019.10:3972314::TTTT 285/58160) Row 532526176 (NC_000019.10:3972314::TTTTT 71/58172)...	-	Apr 26, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532526174 (NC_000019.10:3972314::T 35278/58354) Row 532526175 (NC_000019.10:3972314::TTTT 285/58160) Row 532526176 (NC_000019.10:3972314::TTTTT 71/58172)...	-	Apr 26, 2021 (155)
93	gnomAD - Exomes Submission ignored due to conflicting rows: Row 12792390 (NC_000019.9:3972312::T 2252/13722) Row 12792391 (NC_000019.9:3972312::TT 1523/13722) Row 12792392 (NC_000019.9:3972312::TTT 762/13722)...	-	Jul 13, 2019 (153)
94	gnomAD - Exomes Submission ignored due to conflicting rows: Row 12792390 (NC_000019.9:3972312::T 2252/13722) Row 12792391 (NC_000019.9:3972312::TT 1523/13722) Row 12792392 (NC_000019.9:3972312::TTT 762/13722)...	-	Jul 13, 2019 (153)
95	gnomAD - Exomes Submission ignored due to conflicting rows: Row 12792390 (NC_000019.9:3972312::T 2252/13722) Row 12792391 (NC_000019.9:3972312::TT 1523/13722) Row 12792392 (NC_000019.9:3972312::TTT 762/13722)...	-	Jul 13, 2019 (153)
96	gnomAD - Exomes Submission ignored due to conflicting rows: Row 12792390 (NC_000019.9:3972312::T 2252/13722) Row 12792391 (NC_000019.9:3972312::TT 1523/13722) Row 12792392 (NC_000019.9:3972312::TTT 762/13722)...	-	Jul 13, 2019 (153)
97	gnomAD - Exomes Submission ignored due to conflicting rows: Row 12792390 (NC_000019.9:3972312::T 2252/13722) Row 12792391 (NC_000019.9:3972312::TT 1523/13722) Row 12792392 (NC_000019.9:3972312::TTT 762/13722)...	-	Jul 13, 2019 (153)
98	gnomAD - Exomes Submission ignored due to conflicting rows: Row 12792390 (NC_000019.9:3972312::T 2252/13722) Row 12792391 (NC_000019.9:3972312::TT 1523/13722) Row 12792392 (NC_000019.9:3972312::TTT 762/13722)...	-	Jul 13, 2019 (153)
99	8.3KJPN Submission ignored due to conflicting rows: Row 84434001 (NC_000019.9:3972312::T 7502/15938) Row 84434002 (NC_000019.9:3972312::TT 1238/15938) Row 84434003 (NC_000019.9:3972312::TTT 227/15938)...	-	Apr 26, 2021 (155)
100	8.3KJPN Submission ignored due to conflicting rows: Row 84434001 (NC_000019.9:3972312::T 7502/15938) Row 84434002 (NC_000019.9:3972312::TT 1238/15938) Row 84434003 (NC_000019.9:3972312::TTT 227/15938)...	-	Apr 26, 2021 (155)
101	8.3KJPN Submission ignored due to conflicting rows: Row 84434001 (NC_000019.9:3972312::T 7502/15938) Row 84434002 (NC_000019.9:3972312::TT 1238/15938) Row 84434003 (NC_000019.9:3972312::TTT 227/15938)...	-	Apr 26, 2021 (155)
102	8.3KJPN Submission ignored due to conflicting rows: Row 84434001 (NC_000019.9:3972312::T 7502/15938) Row 84434002 (NC_000019.9:3972312::TT 1238/15938) Row 84434003 (NC_000019.9:3972312::TTT 227/15938)...	-	Apr 26, 2021 (155)
103	8.3KJPN Submission ignored due to conflicting rows: Row 84434001 (NC_000019.9:3972312::T 7502/15938) Row 84434002 (NC_000019.9:3972312::TT 1238/15938) Row 84434003 (NC_000019.9:3972312::TTT 227/15938)...	-	Apr 26, 2021 (155)
104	14KJPN Submission ignored due to conflicting rows: Row 118485190 (NC_000019.10:3972314::TT 1959/26046) Row 118485191 (NC_000019.10:3972314::T 12655/26046) Row 118485192 (NC_000019.10:3972314::TTT 316/26046)...	-	Oct 16, 2022 (156)
105	14KJPN Submission ignored due to conflicting rows: Row 118485190 (NC_000019.10:3972314::TT 1959/26046) Row 118485191 (NC_000019.10:3972314::T 12655/26046) Row 118485192 (NC_000019.10:3972314::TTT 316/26046)...	-	Oct 16, 2022 (156)
106	14KJPN Submission ignored due to conflicting rows: Row 118485190 (NC_000019.10:3972314::TT 1959/26046) Row 118485191 (NC_000019.10:3972314::T 12655/26046) Row 118485192 (NC_000019.10:3972314::TTT 316/26046)...	-	Oct 16, 2022 (156)
107	14KJPN Submission ignored due to conflicting rows: Row 118485190 (NC_000019.10:3972314::TT 1959/26046) Row 118485191 (NC_000019.10:3972314::T 12655/26046) Row 118485192 (NC_000019.10:3972314::TTT 316/26046)...	-	Oct 16, 2022 (156)
108	14KJPN Submission ignored due to conflicting rows: Row 118485190 (NC_000019.10:3972314::TT 1959/26046) Row 118485191 (NC_000019.10:3972314::T 12655/26046) Row 118485192 (NC_000019.10:3972314::TTT 316/26046)...	-	Oct 16, 2022 (156)
109	UK 10K study - Twins	NC_000019.9 - 3972313	Oct 12, 2018 (152)
110	ALFA	NC_000019.10 - 3972315	Apr 26, 2021 (155)

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

Associated ID	History Updated (Build)
rs147966536	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4326724670	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTT:	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTT	(self)
ss4326724669	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTT:	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
7674381010	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4326724668	NC_000019.10:3972314:TTTTTTTTTTTTT:	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
7674381010	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4326724667	NC_000019.10:3972314:TTTTTTTTTTTT:	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
7674381010	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4326724666	NC_000019.10:3972314:TTTTTTTTTTT:	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
7674381010	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4326724665	NC_000019.10:3972314:TTTTTTTTTT:	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
7674381010	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4326724664	NC_000019.10:3972314:TTTTTTTTT:	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
7674381010	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4326724663	NC_000019.10:3972314:TTTTTTTT:	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
7674381010	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4326724662	NC_000019.10:3972314:TTTTTTT:	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
7674381010	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4326724661	NC_000019.10:3972314:TTTTTT:	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
7674381010	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4326724660	NC_000019.10:3972314:TTTTT:	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
7674381010	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3016997959, ss3984139409, ss5226464698	NC_000019.9:3972312:TTTT:	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4326724659, ss5306291112	NC_000019.10:3972314:TTTT:	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
7674381010	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4326724658, ss5784648090	NC_000019.10:3972314:TTT:	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
7674381010	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
	NC_000019.9:3972312:TT:	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4326724657	NC_000019.10:3972314:TT:	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
7674381010	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
	NC_000019.9:3972312:T:	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5306291111	NC_000019.10:3972314:T:	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
7674381010	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss294951674	NC_000019.8:3923337::T	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
41848805, 615899, 41848805, ss664442695, ss1575221902, ss1709098601, ss1709098610, ss1712178572, ss5226464694, ss5953294781	NC_000019.9:3972312::T	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4326724643, ss5784648087	NC_000019.10:3972314::T	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
7674381010	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss41027229	NT_011255.14:3912312::T	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss1712178570, ss5226464695, ss5840177335	NC_000019.9:3972312::TT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5784648086	NC_000019.10:3972314::TT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
7674381010	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss1712178573, ss5226464696, ss5840177334	NC_000019.9:3972312::TTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5306291109, ss5784648088	NC_000019.10:3972314::TTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
7674381010	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss1712178571, ss5226464697	NC_000019.9:3972312::TTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4326724644, ss5306291110, ss5784648089	NC_000019.10:3972314::TTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
7674381010	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss1712178574	NC_000019.9:3972312::TTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4326724645	NC_000019.10:3972314::TTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4326724646	NC_000019.10:3972314::TTTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
7674381010	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4326724647	NC_000019.10:3972314::TTTTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
7674381010	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4326724648	NC_000019.10:3972314::TTTTTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4326724649	NC_000019.10:3972314::TTTTTTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4326724650	NC_000019.10:3972314::TTTTTTTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4326724651	NC_000019.10:3972314::TTTTTTTTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4326724652	NC_000019.10:3972314::TTTTTTTTTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4326724653	NC_000019.10:3972314::TTTTTTTTTTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4326724654	NC_000019.10:3972314::TTTTTTTTTTTT… NC_000019.10:3972314::TTTTTTTTTTTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4326724655	NC_000019.10:3972314::TTTTTTTTTTTT… NC_000019.10:3972314::TTTTTTTTTTTTTTT	NC_000019.10:3972314:TTTTTTTTTTTTT… NC_000019.10:3972314:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs34972570

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs34972570