Name: rs11344697
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.

rs11344697

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr17:50709590-50709611 (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)₁₃ / del(T)₇ / del(T)₆ / del…
del(T)₁₃ / 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 / ins(T)₃₀ / ins(T)₃₄
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₁₃=0.000015 (4/264690, TOPMED)
delT=0.08528 (912/10694, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ANKRD40 : 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	10694	TTTTTTTTTTTTTTTTTTTTTT=0.90340	TTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00159, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.08528, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00206, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00327, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00196, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00243, TTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.847425	0.019191	0.133384	32
European	Sub	8244	TTTTTTTTTTTTTTTTTTTTTT=0.8754	TTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0021, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.1101, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0027, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0042, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0025, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0029, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.801931	0.024759	0.17331	33
African	Sub	1986	TTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	86	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1900	TTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	44	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	32	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	12	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	42	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	148	TTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	22	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	208	TTTTTTTTTTTTTTTTTTTTTT=0.971	TTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.019, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.010, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000	0.970874	0.009709	0.019417	14

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
TopMed	Global	Study-wide	264690	(T)₂₂=0.999985	del(T)₁₃=0.000015
Allele Frequency Aggregator	Total	Global	10694	(T)₂₂=0.90340	del(T)₁₃=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.00159, delTT=0.00000, delT=0.08528, dupT=0.00000, dupTT=0.00000, dup(T)₅=0.00243, dup(T)₆=0.00196, dup(T)₇=0.00206, dup(T)₈=0.00327
Allele Frequency Aggregator	European	Sub	8244	(T)₂₂=0.8754	del(T)₁₃=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0021, delTT=0.0000, delT=0.1101, dupT=0.0000, dupTT=0.0000, dup(T)₅=0.0029, dup(T)₆=0.0025, dup(T)₇=0.0027, dup(T)₈=0.0042
Allele Frequency Aggregator	African	Sub	1986	(T)₂₂=1.0000	del(T)₁₃=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dup(T)₅=0.0000, dup(T)₆=0.0000, dup(T)₇=0.0000, dup(T)₈=0.0000
Allele Frequency Aggregator	Other	Sub	208	(T)₂₂=0.971	del(T)₁₃=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=0.019, dupT=0.000, dupTT=0.000, dup(T)₅=0.010, dup(T)₆=0.000, dup(T)₇=0.000, dup(T)₈=0.000
Allele Frequency Aggregator	Latin American 2	Sub	148	(T)₂₂=1.000	del(T)₁₃=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, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000, dup(T)₈=0.000
Allele Frequency Aggregator	Asian	Sub	44	(T)₂₂=1.00	del(T)₁₃=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, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00
Allele Frequency Aggregator	Latin American 1	Sub	42	(T)₂₂=1.00	del(T)₁₃=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, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00
Allele Frequency Aggregator	South Asian	Sub	22	(T)₂₂=1.00	del(T)₁₃=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, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 17	NC_000017.11:g.50709599_50709611del
GRCh38.p14 chr 17	NC_000017.11:g.50709605_50709611del
GRCh38.p14 chr 17	NC_000017.11:g.50709606_50709611del
GRCh38.p14 chr 17	NC_000017.11:g.50709607_50709611del
GRCh38.p14 chr 17	NC_000017.11:g.50709608_50709611del
GRCh38.p14 chr 17	NC_000017.11:g.50709609_50709611del
GRCh38.p14 chr 17	NC_000017.11:g.50709610_50709611del
GRCh38.p14 chr 17	NC_000017.11:g.50709611del
GRCh38.p14 chr 17	NC_000017.11:g.50709611dup
GRCh38.p14 chr 17	NC_000017.11:g.50709610_50709611dup
GRCh38.p14 chr 17	NC_000017.11:g.50709609_50709611dup
GRCh38.p14 chr 17	NC_000017.11:g.50709608_50709611dup
GRCh38.p14 chr 17	NC_000017.11:g.50709607_50709611dup
GRCh38.p14 chr 17	NC_000017.11:g.50709606_50709611dup
GRCh38.p14 chr 17	NC_000017.11:g.50709605_50709611dup
GRCh38.p14 chr 17	NC_000017.11:g.50709604_50709611dup
GRCh38.p14 chr 17	NC_000017.11:g.50709603_50709611dup
GRCh38.p14 chr 17	NC_000017.11:g.50709602_50709611dup
GRCh38.p14 chr 17	NC_000017.11:g.50709601_50709611dup
GRCh38.p14 chr 17	NC_000017.11:g.50709611_50709612insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 17	NC_000017.11:g.50709611_50709612insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 17	NC_000017.10:g.48786960_48786972del
GRCh37.p13 chr 17	NC_000017.10:g.48786966_48786972del
GRCh37.p13 chr 17	NC_000017.10:g.48786967_48786972del
GRCh37.p13 chr 17	NC_000017.10:g.48786968_48786972del
GRCh37.p13 chr 17	NC_000017.10:g.48786969_48786972del
GRCh37.p13 chr 17	NC_000017.10:g.48786970_48786972del
GRCh37.p13 chr 17	NC_000017.10:g.48786971_48786972del
GRCh37.p13 chr 17	NC_000017.10:g.48786972del
GRCh37.p13 chr 17	NC_000017.10:g.48786972dup
GRCh37.p13 chr 17	NC_000017.10:g.48786971_48786972dup
GRCh37.p13 chr 17	NC_000017.10:g.48786970_48786972dup
GRCh37.p13 chr 17	NC_000017.10:g.48786969_48786972dup
GRCh37.p13 chr 17	NC_000017.10:g.48786968_48786972dup
GRCh37.p13 chr 17	NC_000017.10:g.48786967_48786972dup
GRCh37.p13 chr 17	NC_000017.10:g.48786966_48786972dup
GRCh37.p13 chr 17	NC_000017.10:g.48786965_48786972dup
GRCh37.p13 chr 17	NC_000017.10:g.48786964_48786972dup
GRCh37.p13 chr 17	NC_000017.10:g.48786963_48786972dup
GRCh37.p13 chr 17	NC_000017.10:g.48786962_48786972dup
GRCh37.p13 chr 17	NC_000017.10:g.48786972_48786973insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 17	NC_000017.10:g.48786972_48786973insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: ANKRD40, ankyrin repeat domain 40 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
ANKRD40 transcript	NM_052855.4: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)₂₂=	del(T)₁₃	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	ins(T)₃₀	ins(T)₃₄
GRCh38.p14 chr 17	NC_000017.11:g.50709590_50709611=	NC_000017.11:g.50709599_50709611del	NC_000017.11:g.50709605_50709611del	NC_000017.11:g.50709606_50709611del	NC_000017.11:g.50709607_50709611del	NC_000017.11:g.50709608_50709611del	NC_000017.11:g.50709609_50709611del	NC_000017.11:g.50709610_50709611del	NC_000017.11:g.50709611del	NC_000017.11:g.50709611dup	NC_000017.11:g.50709610_50709611dup	NC_000017.11:g.50709609_50709611dup	NC_000017.11:g.50709608_50709611dup	NC_000017.11:g.50709607_50709611dup	NC_000017.11:g.50709606_50709611dup	NC_000017.11:g.50709605_50709611dup	NC_000017.11:g.50709604_50709611dup	NC_000017.11:g.50709603_50709611dup	NC_000017.11:g.50709602_50709611dup	NC_000017.11:g.50709601_50709611dup	NC_000017.11:g.50709611_50709612insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:g.50709611_50709612insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 17	NC_000017.10:g.48786951_48786972=	NC_000017.10:g.48786960_48786972del	NC_000017.10:g.48786966_48786972del	NC_000017.10:g.48786967_48786972del	NC_000017.10:g.48786968_48786972del	NC_000017.10:g.48786969_48786972del	NC_000017.10:g.48786970_48786972del	NC_000017.10:g.48786971_48786972del	NC_000017.10:g.48786972del	NC_000017.10:g.48786972dup	NC_000017.10:g.48786971_48786972dup	NC_000017.10:g.48786970_48786972dup	NC_000017.10:g.48786969_48786972dup	NC_000017.10:g.48786968_48786972dup	NC_000017.10:g.48786967_48786972dup	NC_000017.10:g.48786966_48786972dup	NC_000017.10:g.48786965_48786972dup	NC_000017.10:g.48786964_48786972dup	NC_000017.10:g.48786963_48786972dup	NC_000017.10:g.48786962_48786972dup	NC_000017.10:g.48786972_48786973insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.10:g.48786972_48786973insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

43 SubSNP, 26 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40770484	Dec 03, 2013 (142)
2	HGSV	ss81687512	Dec 14, 2007 (130)
3	PJP	ss294916148	May 09, 2011 (134)
4	SWEGEN	ss3015628504	Nov 08, 2017 (151)
5	PACBIO	ss3788222507	Jul 13, 2019 (153)
6	PACBIO	ss3793176706	Jul 13, 2019 (153)
7	PACBIO	ss3798062491	Jul 13, 2019 (153)
8	EVA	ss3834894940	Apr 27, 2020 (154)
9	GNOMAD	ss4312588977	Apr 26, 2021 (155)
10	GNOMAD	ss4312588978	Apr 26, 2021 (155)
11	GNOMAD	ss4312588979	Apr 26, 2021 (155)
12	GNOMAD	ss4312588982	Apr 26, 2021 (155)
13	GNOMAD	ss4312588983	Apr 26, 2021 (155)
14	GNOMAD	ss4312588984	Apr 26, 2021 (155)
15	GNOMAD	ss4312588985	Apr 26, 2021 (155)
16	GNOMAD	ss4312588986	Apr 26, 2021 (155)
17	GNOMAD	ss4312588987	Apr 26, 2021 (155)
18	GNOMAD	ss4312588988	Apr 26, 2021 (155)
19	GNOMAD	ss4312588989	Apr 26, 2021 (155)
20	GNOMAD	ss4312588990	Apr 26, 2021 (155)
21	GNOMAD	ss4312588991	Apr 26, 2021 (155)
22	GNOMAD	ss4312588992	Apr 26, 2021 (155)
23	GNOMAD	ss4312588993	Apr 26, 2021 (155)
24	GNOMAD	ss4312588994	Apr 26, 2021 (155)
25	GNOMAD	ss4312588995	Apr 26, 2021 (155)
26	GNOMAD	ss4312588996	Apr 26, 2021 (155)
27	TOPMED	ss5037849426	Apr 26, 2021 (155)
28	TOMMO_GENOMICS	ss5222687777	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5222687778	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5222687779	Apr 26, 2021 (155)
31	1000G_HIGH_COVERAGE	ss5303325653	Oct 16, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5303325654	Oct 16, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5303325655	Oct 16, 2022 (156)
34	HUGCELL_USP	ss5496353128	Oct 16, 2022 (156)
35	HUGCELL_USP	ss5496353129	Oct 16, 2022 (156)
36	HUGCELL_USP	ss5496353130	Oct 16, 2022 (156)
37	HUGCELL_USP	ss5496353131	Oct 16, 2022 (156)
38	TOMMO_GENOMICS	ss5778985932	Oct 16, 2022 (156)
39	TOMMO_GENOMICS	ss5778985934	Oct 16, 2022 (156)
40	TOMMO_GENOMICS	ss5778985935	Oct 16, 2022 (156)
41	EVA	ss5834058858	Oct 16, 2022 (156)
42	EVA	ss5834058859	Oct 16, 2022 (156)
43	EVA	ss5834058860	Oct 16, 2022 (156)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508863881 (NC_000017.11:50709589::T 601/81222) Row 508863882 (NC_000017.11:50709589::TT 284/81222) Row 508863883 (NC_000017.11:50709589::TTT 93/81242)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508863881 (NC_000017.11:50709589::T 601/81222) Row 508863882 (NC_000017.11:50709589::TT 284/81222) Row 508863883 (NC_000017.11:50709589::TTT 93/81242)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508863881 (NC_000017.11:50709589::T 601/81222) Row 508863882 (NC_000017.11:50709589::TT 284/81222) Row 508863883 (NC_000017.11:50709589::TTT 93/81242)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508863881 (NC_000017.11:50709589::T 601/81222) Row 508863882 (NC_000017.11:50709589::TT 284/81222) Row 508863883 (NC_000017.11:50709589::TTT 93/81242)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508863881 (NC_000017.11:50709589::T 601/81222) Row 508863882 (NC_000017.11:50709589::TT 284/81222) Row 508863883 (NC_000017.11:50709589::TTT 93/81242)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508863881 (NC_000017.11:50709589::T 601/81222) Row 508863882 (NC_000017.11:50709589::TT 284/81222) Row 508863883 (NC_000017.11:50709589::TTT 93/81242)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508863881 (NC_000017.11:50709589::T 601/81222) Row 508863882 (NC_000017.11:50709589::TT 284/81222) Row 508863883 (NC_000017.11:50709589::TTT 93/81242)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508863881 (NC_000017.11:50709589::T 601/81222) Row 508863882 (NC_000017.11:50709589::TT 284/81222) Row 508863883 (NC_000017.11:50709589::TTT 93/81242)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508863881 (NC_000017.11:50709589::T 601/81222) Row 508863882 (NC_000017.11:50709589::TT 284/81222) Row 508863883 (NC_000017.11:50709589::TTT 93/81242)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508863881 (NC_000017.11:50709589::T 601/81222) Row 508863882 (NC_000017.11:50709589::TT 284/81222) Row 508863883 (NC_000017.11:50709589::TTT 93/81242)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508863881 (NC_000017.11:50709589::T 601/81222) Row 508863882 (NC_000017.11:50709589::TT 284/81222) Row 508863883 (NC_000017.11:50709589::TTT 93/81242)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508863881 (NC_000017.11:50709589::T 601/81222) Row 508863882 (NC_000017.11:50709589::TT 284/81222) Row 508863883 (NC_000017.11:50709589::TTT 93/81242)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508863881 (NC_000017.11:50709589::T 601/81222) Row 508863882 (NC_000017.11:50709589::TT 284/81222) Row 508863883 (NC_000017.11:50709589::TTT 93/81242)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508863881 (NC_000017.11:50709589::T 601/81222) Row 508863882 (NC_000017.11:50709589::TT 284/81222) Row 508863883 (NC_000017.11:50709589::TTT 93/81242)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508863881 (NC_000017.11:50709589::T 601/81222) Row 508863882 (NC_000017.11:50709589::TT 284/81222) Row 508863883 (NC_000017.11:50709589::TTT 93/81242)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508863881 (NC_000017.11:50709589::T 601/81222) Row 508863882 (NC_000017.11:50709589::TT 284/81222) Row 508863883 (NC_000017.11:50709589::TTT 93/81242)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508863881 (NC_000017.11:50709589::T 601/81222) Row 508863882 (NC_000017.11:50709589::TT 284/81222) Row 508863883 (NC_000017.11:50709589::TTT 93/81242)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508863881 (NC_000017.11:50709589::T 601/81222) Row 508863882 (NC_000017.11:50709589::TT 284/81222) Row 508863883 (NC_000017.11:50709589::TTT 93/81242)...	-	Apr 26, 2021 (155)
62	8.3KJPN Submission ignored due to conflicting rows: Row 80657084 (NC_000017.10:48786950:T: 4685/16308) Row 80657085 (NC_000017.10:48786950:TT: 18/16308) Row 80657086 (NC_000017.10:48786950::T 18/16308)	-	Apr 26, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 80657084 (NC_000017.10:48786950:T: 4685/16308) Row 80657085 (NC_000017.10:48786950:TT: 18/16308) Row 80657086 (NC_000017.10:48786950::T 18/16308)	-	Apr 26, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 80657084 (NC_000017.10:48786950:T: 4685/16308) Row 80657085 (NC_000017.10:48786950:TT: 18/16308) Row 80657086 (NC_000017.10:48786950::T 18/16308)	-	Apr 26, 2021 (155)
65	14KJPN Submission ignored due to conflicting rows: Row 112823036 (NC_000017.11:50709589:T: 9487/27732) Row 112823038 (NC_000017.11:50709589:TT: 29/27732) Row 112823039 (NC_000017.11:50709589::T 30/27732)	-	Oct 16, 2022 (156)
66	14KJPN Submission ignored due to conflicting rows: Row 112823036 (NC_000017.11:50709589:T: 9487/27732) Row 112823038 (NC_000017.11:50709589:TT: 29/27732) Row 112823039 (NC_000017.11:50709589::T 30/27732)	-	Oct 16, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 112823036 (NC_000017.11:50709589:T: 9487/27732) Row 112823038 (NC_000017.11:50709589:TT: 29/27732) Row 112823039 (NC_000017.11:50709589::T 30/27732)	-	Oct 16, 2022 (156)
68	TopMed	NC_000017.11 - 50709590	Apr 26, 2021 (155)
69	ALFA	NC_000017.11 - 50709590	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)
rs56903374	May 23, 2008 (130)
rs397856560	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
253395088, ss4312588996, ss5037849426	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTT:	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
1494869985	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss4312588995	NC_000017.11:50709589:TTTTTTT:	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
1494869985	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
1494869985	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4312588994	NC_000017.11:50709589:TTTTT:	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
1494869985	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
1494869985	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3015628504, ss5834058860	NC_000017.10:48786950:TTT:	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4312588993, ss5303325655, ss5496353131	NC_000017.11:50709589:TTT:	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
1494869985	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3788222507, ss5222687778, ss5834058859	NC_000017.10:48786950:TT:	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4312588992, ss5303325654, ss5496353130, ss5778985934	NC_000017.11:50709589:TT:	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
1494869985	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss81687512, ss294916148	NC_000017.9:46141970:T:	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3793176706, ss3798062491, ss3834894940, ss5222687777, ss5834058858	NC_000017.10:48786950:T:	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss5496353128, ss5778985932	NC_000017.11:50709589:T:	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
1494869985	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss40770484	NT_010783.15:14061123:T:	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss5222687779	NC_000017.10:48786950::T	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4312588977, ss5303325653, ss5496353129, ss5778985935	NC_000017.11:50709589::T	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
1494869985	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4312588978	NC_000017.11:50709589::TT	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
1494869985	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4312588979	NC_000017.11:50709589::TTT	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4312588982	NC_000017.11:50709589::TTTT	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4312588983	NC_000017.11:50709589::TTTTT	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
1494869985	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4312588984	NC_000017.11:50709589::TTTTTT	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
1494869985	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4312588985	NC_000017.11:50709589::TTTTTTT	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
1494869985	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4312588986	NC_000017.11:50709589::TTTTTTTT	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
1494869985	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4312588987	NC_000017.11:50709589::TTTTTTTTT	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4312588988	NC_000017.11:50709589::TTTTTTTTTT	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4312588989	NC_000017.11:50709589::TTTTTTTTTTT	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4312588990	NC_000017.11:50709589::TTTTTTTTTTT… NC_000017.11:50709589::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4312588991	NC_000017.11:50709589::TTTTTTTTTTT… NC_000017.11:50709589::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2382406989	NC_000017.10:48786950:TTTTTTTTTTTT… NC_000017.10:48786950:TTTTTTTTTTTTT:	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT
ss3264298429	NC_000017.11:50709589:TTTT:	NC_000017.11:50709589:TTTTTTTTTTTT… NC_000017.11:50709589:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT

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

No publications for rs11344697

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

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs11344697