Name: rs11290690
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.

rs11290690

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:108774641-108774661 (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)₁₂ / del(T)₁₁ / d…
del(T)₁₃ / del(T)₁₂ / del(T)₁₁ / del(T)₈ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dup(T)₄ / dup(T)₆ / ins(T)₆(CTTT)₂TTTTTTTTTTTTTTTTTTTTTTTTTTT / dup(T)₈ / dup(T)₁₀ / ins(T)₂₅
Variation Type: Indel Insertion and Deletion
Frequency: (T)₂₁=0.4818 (2413/5008, 1000G)
delT=0.2615 (1178/4504, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: STXBP3 : 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	Alt HMOZ	HTRZ	HWEP
Total	Global	4504	TTTTTTTTTTTTTTTTTTTTT=0.4891	TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.1317, TTTTTTTTTTTTTTTTTTT=0.1132, TTTTTTTTTTTTTTTTTTTT=0.2615, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0027, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0018, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.607278	0.124337	0.268385	32
European	Sub	4480	TTTTTTTTTTTTTTTTTTTTT=0.4875	TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.1321, TTTTTTTTTTTTTTTTTTT=0.1138, TTTTTTTTTTTTTTTTTTTT=0.2621, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0027, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0018, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.605505	0.124618	0.269878	32
African	Sub	16	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African Others	Sub	0	TTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTT=0, TTTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
African American	Sub	16	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Asian	Sub	0	TTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTT=0, TTTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
East Asian	Sub	0	TTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTT=0, TTTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTT=0, TTTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	0	TTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTT=0, TTTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 2	Sub	0	TTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTT=0, TTTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
South Asian	Sub	0	TTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTT=0, TTTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Other	Sub	8	TTTTTTTTTTTTTTTTTTTTT=0.4	TTTTTTTT=0.0, TTTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.1, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.5, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0	0.333333	0.333333	0.333333	0

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
1000Genomes	Global	Study-wide	5008	(T)₂₁=0.4818	delT=0.5182
1000Genomes	African	Sub	1322	(T)₂₁=0.6399	delT=0.3601
1000Genomes	East Asian	Sub	1008	(T)₂₁=0.4177	delT=0.5823
1000Genomes	Europe	Sub	1006	(T)₂₁=0.4453	delT=0.5547
1000Genomes	South Asian	Sub	978	(T)₂₁=0.395	delT=0.605
1000Genomes	American	Sub	694	(T)₂₁=0.450	delT=0.550
Allele Frequency Aggregator	Total	Global	4504	(T)₂₁=0.4891	del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₈=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.1317, delTT=0.1132, delT=0.2615, dupT=0.0000, dupTT=0.0000, dup(T)₆=0.0027, dup(T)₁₀=0.0018
Allele Frequency Aggregator	European	Sub	4480	(T)₂₁=0.4875	del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₈=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.1321, delTT=0.1138, delT=0.2621, dupT=0.0000, dupTT=0.0000, dup(T)₆=0.0027, dup(T)₁₀=0.0018
Allele Frequency Aggregator	African	Sub	16	(T)₂₁=1.00	del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₈=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)₆=0.00, dup(T)₁₀=0.00
Allele Frequency Aggregator	Other	Sub	8	(T)₂₁=0.4	del(T)₁₃=0.0, del(T)₁₂=0.0, del(T)₁₁=0.0, del(T)₈=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.1, delTT=0.0, delT=0.5, dupT=0.0, dupTT=0.0, dup(T)₆=0.0, dup(T)₁₀=0.0
Allele Frequency Aggregator	Latin American 1	Sub	0	(T)₂₁=0	del(T)₁₃=0, del(T)₁₂=0, del(T)₁₁=0, del(T)₈=0, del(T)₅=0, del(T)₄=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dup(T)₆=0, dup(T)₁₀=0
Allele Frequency Aggregator	Latin American 2	Sub	0	(T)₂₁=0	del(T)₁₃=0, del(T)₁₂=0, del(T)₁₁=0, del(T)₈=0, del(T)₅=0, del(T)₄=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dup(T)₆=0, dup(T)₁₀=0
Allele Frequency Aggregator	South Asian	Sub	0	(T)₂₁=0	del(T)₁₃=0, del(T)₁₂=0, del(T)₁₁=0, del(T)₈=0, del(T)₅=0, del(T)₄=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dup(T)₆=0, dup(T)₁₀=0
Allele Frequency Aggregator	Asian	Sub	0	(T)₂₁=0	del(T)₁₃=0, del(T)₁₂=0, del(T)₁₁=0, del(T)₈=0, del(T)₅=0, del(T)₄=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dup(T)₆=0, dup(T)₁₀=0

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 1	NC_000001.11:g.108774649_108774661del
GRCh38.p14 chr 1	NC_000001.11:g.108774650_108774661del
GRCh38.p14 chr 1	NC_000001.11:g.108774651_108774661del
GRCh38.p14 chr 1	NC_000001.11:g.108774654_108774661del
GRCh38.p14 chr 1	NC_000001.11:g.108774656_108774661del
GRCh38.p14 chr 1	NC_000001.11:g.108774657_108774661del
GRCh38.p14 chr 1	NC_000001.11:g.108774658_108774661del
GRCh38.p14 chr 1	NC_000001.11:g.108774659_108774661del
GRCh38.p14 chr 1	NC_000001.11:g.108774660_108774661del
GRCh38.p14 chr 1	NC_000001.11:g.108774661del
GRCh38.p14 chr 1	NC_000001.11:g.108774661dup
GRCh38.p14 chr 1	NC_000001.11:g.108774660_108774661dup
GRCh38.p14 chr 1	NC_000001.11:g.108774658_108774661dup
GRCh38.p14 chr 1	NC_000001.11:g.108774656_108774661dup
GRCh38.p14 chr 1	NC_000001.11:g.108774641_108774661T[27]CTTT[2]T[27]
GRCh38.p14 chr 1	NC_000001.11:g.108774654_108774661dup
GRCh38.p14 chr 1	NC_000001.11:g.108774652_108774661dup
GRCh38.p14 chr 1	NC_000001.11:g.108774661_108774662insTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.109317271_109317283del
GRCh37.p13 chr 1	NC_000001.10:g.109317272_109317283del
GRCh37.p13 chr 1	NC_000001.10:g.109317273_109317283del
GRCh37.p13 chr 1	NC_000001.10:g.109317276_109317283del
GRCh37.p13 chr 1	NC_000001.10:g.109317278_109317283del
GRCh37.p13 chr 1	NC_000001.10:g.109317279_109317283del
GRCh37.p13 chr 1	NC_000001.10:g.109317280_109317283del
GRCh37.p13 chr 1	NC_000001.10:g.109317281_109317283del
GRCh37.p13 chr 1	NC_000001.10:g.109317282_109317283del
GRCh37.p13 chr 1	NC_000001.10:g.109317283del
GRCh37.p13 chr 1	NC_000001.10:g.109317283dup
GRCh37.p13 chr 1	NC_000001.10:g.109317282_109317283dup
GRCh37.p13 chr 1	NC_000001.10:g.109317280_109317283dup
GRCh37.p13 chr 1	NC_000001.10:g.109317278_109317283dup
GRCh37.p13 chr 1	NC_000001.10:g.109317263_109317283T[27]CTTT[2]T[27]
GRCh37.p13 chr 1	NC_000001.10:g.109317276_109317283dup
GRCh37.p13 chr 1	NC_000001.10:g.109317274_109317283dup
GRCh37.p13 chr 1	NC_000001.10:g.109317283_109317284insTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: STXBP3, syntaxin binding protein 3 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
STXBP3 transcript	NM_007269.4:c.594-1684_59… NM_007269.4:c.594-1684_594-1672del	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	(T)₂₁=	del(T)₁₃	del(T)₁₂	del(T)₁₁	del(T)₈	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dup(T)₄	dup(T)₆	ins(T)₆(CTTT)₂TTTTTTTTTTTTTTTTTTTTTTTTTTT	dup(T)₈	dup(T)₁₀	ins(T)₂₅
GRCh38.p14 chr 1	NC_000001.11:g.108774641_108774661=	NC_000001.11:g.108774649_108774661del	NC_000001.11:g.108774650_108774661del	NC_000001.11:g.108774651_108774661del	NC_000001.11:g.108774654_108774661del	NC_000001.11:g.108774656_108774661del	NC_000001.11:g.108774657_108774661del	NC_000001.11:g.108774658_108774661del	NC_000001.11:g.108774659_108774661del	NC_000001.11:g.108774660_108774661del	NC_000001.11:g.108774661del	NC_000001.11:g.108774661dup	NC_000001.11:g.108774660_108774661dup	NC_000001.11:g.108774658_108774661dup	NC_000001.11:g.108774656_108774661dup	NC_000001.11:g.108774641_108774661T[27]CTTT[2]T[27]	NC_000001.11:g.108774654_108774661dup	NC_000001.11:g.108774652_108774661dup	NC_000001.11:g.108774661_108774662insTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.109317263_109317283=	NC_000001.10:g.109317271_109317283del	NC_000001.10:g.109317272_109317283del	NC_000001.10:g.109317273_109317283del	NC_000001.10:g.109317276_109317283del	NC_000001.10:g.109317278_109317283del	NC_000001.10:g.109317279_109317283del	NC_000001.10:g.109317280_109317283del	NC_000001.10:g.109317281_109317283del	NC_000001.10:g.109317282_109317283del	NC_000001.10:g.109317283del	NC_000001.10:g.109317283dup	NC_000001.10:g.109317282_109317283dup	NC_000001.10:g.109317280_109317283dup	NC_000001.10:g.109317278_109317283dup	NC_000001.10:g.109317263_109317283T[27]CTTT[2]T[27]	NC_000001.10:g.109317276_109317283dup	NC_000001.10:g.109317274_109317283dup	NC_000001.10:g.109317283_109317284insTTTTTTTTTTTTTTTTTTTTTTTTT
STXBP3 transcript	NM_007269.2:c.594-1692=	NM_007269.2:c.594-1684_594-1672del	NM_007269.2:c.594-1683_594-1672del	NM_007269.2:c.594-1682_594-1672del	NM_007269.2:c.594-1679_594-1672del	NM_007269.2:c.594-1677_594-1672del	NM_007269.2:c.594-1676_594-1672del	NM_007269.2:c.594-1675_594-1672del	NM_007269.2:c.594-1674_594-1672del	NM_007269.2:c.594-1673_594-1672del	NM_007269.2:c.594-1672del	NM_007269.2:c.594-1672dup	NM_007269.2:c.594-1673_594-1672dup	NM_007269.2:c.594-1675_594-1672dup	NM_007269.2:c.594-1677_594-1672dup	NM_007269.2:c.594-1672_594-1671insTTTTTTCTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_007269.2:c.594-1679_594-1672dup	NM_007269.2:c.594-1681_594-1672dup	NM_007269.2:c.594-1672_594-1671insTTTTTTTTTTTTTTTTTTTTTTTTT
STXBP3 transcript	NM_007269.4:c.594-1692=	NM_007269.4:c.594-1684_594-1672del	NM_007269.4:c.594-1683_594-1672del	NM_007269.4:c.594-1682_594-1672del	NM_007269.4:c.594-1679_594-1672del	NM_007269.4:c.594-1677_594-1672del	NM_007269.4:c.594-1676_594-1672del	NM_007269.4:c.594-1675_594-1672del	NM_007269.4:c.594-1674_594-1672del	NM_007269.4:c.594-1673_594-1672del	NM_007269.4:c.594-1672del	NM_007269.4:c.594-1672dup	NM_007269.4:c.594-1673_594-1672dup	NM_007269.4:c.594-1675_594-1672dup	NM_007269.4:c.594-1677_594-1672dup	NM_007269.4:c.594-1672_594-1671insTTTTTTCTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_007269.4:c.594-1679_594-1672dup	NM_007269.4:c.594-1681_594-1672dup	NM_007269.4:c.594-1672_594-1671insTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

50 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41154319	Mar 13, 2006 (137)
2	HGSV	ss77937236	Dec 06, 2007 (129)
3	HUMANGENOME_JCVI	ss95239894	Feb 05, 2009 (130)
4	PJP	ss294597632	May 09, 2011 (134)
5	1000GENOMES	ss1367811428	Aug 21, 2014 (142)
6	EVA_UK10K_ALSPAC	ss1701083550	Apr 01, 2015 (144)
7	EVA_UK10K_TWINSUK	ss1701083719	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1709943971	Apr 01, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1709943972	Apr 01, 2015 (144)
10	HAMMER_LAB	ss1794905694	Sep 08, 2015 (146)
11	SWEGEN	ss2987410761	Nov 08, 2017 (151)
12	MCHAISSO	ss3065320845	Nov 08, 2017 (151)
13	MCHAISSO	ss3065320846	Nov 08, 2017 (151)
14	EVA_DECODE	ss3687496607	Jul 12, 2019 (153)
15	EVA_DECODE	ss3687496608	Jul 12, 2019 (153)
16	EVA_DECODE	ss3687496609	Jul 12, 2019 (153)
17	EVA_DECODE	ss3687496610	Jul 12, 2019 (153)
18	EVA_DECODE	ss3687496611	Jul 12, 2019 (153)
19	PACBIO	ss3783514679	Jul 12, 2019 (153)
20	PACBIO	ss3789157311	Jul 12, 2019 (153)
21	PACBIO	ss3794030216	Jul 12, 2019 (153)
22	PACBIO	ss3794030217	Jul 12, 2019 (153)
23	KHV_HUMAN_GENOMES	ss3799656031	Jul 12, 2019 (153)
24	GNOMAD	ss4000147787	Apr 25, 2021 (155)
25	GNOMAD	ss4000147788	Apr 25, 2021 (155)
26	GNOMAD	ss4000147789	Apr 25, 2021 (155)
27	GNOMAD	ss4000147790	Apr 25, 2021 (155)
28	GNOMAD	ss4000147791	Apr 25, 2021 (155)
29	GNOMAD	ss4000147792	Apr 25, 2021 (155)
30	GNOMAD	ss4000147793	Apr 25, 2021 (155)
31	GNOMAD	ss4000147794	Apr 25, 2021 (155)
32	GNOMAD	ss4000147795	Apr 25, 2021 (155)
33	GNOMAD	ss4000147796	Apr 25, 2021 (155)
34	GNOMAD	ss4000147797	Apr 25, 2021 (155)
35	TOMMO_GENOMICS	ss5145604980	Apr 25, 2021 (155)
36	TOMMO_GENOMICS	ss5145604981	Apr 25, 2021 (155)
37	TOMMO_GENOMICS	ss5145604982	Apr 25, 2021 (155)
38	1000G_HIGH_COVERAGE	ss5243552156	Oct 12, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5243552157	Oct 12, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5243552158	Oct 12, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5243552159	Oct 12, 2022 (156)
42	HUGCELL_USP	ss5444481262	Oct 12, 2022 (156)
43	HUGCELL_USP	ss5444481263	Oct 12, 2022 (156)
44	HUGCELL_USP	ss5444481264	Oct 12, 2022 (156)
45	TOMMO_GENOMICS	ss5670849892	Oct 12, 2022 (156)
46	TOMMO_GENOMICS	ss5670849893	Oct 12, 2022 (156)
47	TOMMO_GENOMICS	ss5670849894	Oct 12, 2022 (156)
48	EVA	ss5832460718	Oct 12, 2022 (156)
49	EVA	ss5832460719	Oct 12, 2022 (156)
50	EVA	ss5849061126	Oct 12, 2022 (156)
51	1000Genomes	NC_000001.10 - 109317263	Oct 11, 2018 (152)
52	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 1733642 (NC_000001.10:109317263:T: 2073/3854) Row 1733643 (NC_000001.10:109317262:TTT: 1774/3854)	-	Oct 11, 2018 (152)
53	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 1733642 (NC_000001.10:109317263:T: 2073/3854) Row 1733643 (NC_000001.10:109317262:TTT: 1774/3854)	-	Oct 11, 2018 (152)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22204794 (NC_000001.11:108774640::T 21/84970) Row 22204795 (NC_000001.11:108774640::TT 1/84994) Row 22204796 (NC_000001.11:108774640::TTTT 2/84996)...	-	Apr 25, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22204794 (NC_000001.11:108774640::T 21/84970) Row 22204795 (NC_000001.11:108774640::TT 1/84994) Row 22204796 (NC_000001.11:108774640::TTTT 2/84996)...	-	Apr 25, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22204794 (NC_000001.11:108774640::T 21/84970) Row 22204795 (NC_000001.11:108774640::TT 1/84994) Row 22204796 (NC_000001.11:108774640::TTTT 2/84996)...	-	Apr 25, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22204794 (NC_000001.11:108774640::T 21/84970) Row 22204795 (NC_000001.11:108774640::TT 1/84994) Row 22204796 (NC_000001.11:108774640::TTTT 2/84996)...	-	Apr 25, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22204794 (NC_000001.11:108774640::T 21/84970) Row 22204795 (NC_000001.11:108774640::TT 1/84994) Row 22204796 (NC_000001.11:108774640::TTTT 2/84996)...	-	Apr 25, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22204794 (NC_000001.11:108774640::T 21/84970) Row 22204795 (NC_000001.11:108774640::TT 1/84994) Row 22204796 (NC_000001.11:108774640::TTTT 2/84996)...	-	Apr 25, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22204794 (NC_000001.11:108774640::T 21/84970) Row 22204795 (NC_000001.11:108774640::TT 1/84994) Row 22204796 (NC_000001.11:108774640::TTTT 2/84996)...	-	Apr 25, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22204794 (NC_000001.11:108774640::T 21/84970) Row 22204795 (NC_000001.11:108774640::TT 1/84994) Row 22204796 (NC_000001.11:108774640::TTTT 2/84996)...	-	Apr 25, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22204794 (NC_000001.11:108774640::T 21/84970) Row 22204795 (NC_000001.11:108774640::TT 1/84994) Row 22204796 (NC_000001.11:108774640::TTTT 2/84996)...	-	Apr 25, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22204794 (NC_000001.11:108774640::T 21/84970) Row 22204795 (NC_000001.11:108774640::TT 1/84994) Row 22204796 (NC_000001.11:108774640::TTTT 2/84996)...	-	Apr 25, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22204794 (NC_000001.11:108774640::T 21/84970) Row 22204795 (NC_000001.11:108774640::TT 1/84994) Row 22204796 (NC_000001.11:108774640::TTTT 2/84996)...	-	Apr 25, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 3574287 (NC_000001.10:109317262:TTT: 1980/16190) Row 3574288 (NC_000001.10:109317262:T: 10096/16190) Row 3574289 (NC_000001.10:109317262:TT: 857/16190)	-	Apr 25, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 3574287 (NC_000001.10:109317262:TTT: 1980/16190) Row 3574288 (NC_000001.10:109317262:T: 10096/16190) Row 3574289 (NC_000001.10:109317262:TT: 857/16190)	-	Apr 25, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 3574287 (NC_000001.10:109317262:TTT: 1980/16190) Row 3574288 (NC_000001.10:109317262:T: 10096/16190) Row 3574289 (NC_000001.10:109317262:TT: 857/16190)	-	Apr 25, 2021 (155)
68	14KJPN Submission ignored due to conflicting rows: Row 4686996 (NC_000001.11:108774640:T: 18156/27498) Row 4686997 (NC_000001.11:108774640:TTT: 3634/27498) Row 4686998 (NC_000001.11:108774640:TT: 1517/27498)	-	Oct 12, 2022 (156)
69	14KJPN Submission ignored due to conflicting rows: Row 4686996 (NC_000001.11:108774640:T: 18156/27498) Row 4686997 (NC_000001.11:108774640:TTT: 3634/27498) Row 4686998 (NC_000001.11:108774640:TT: 1517/27498)	-	Oct 12, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 4686996 (NC_000001.11:108774640:T: 18156/27498) Row 4686997 (NC_000001.11:108774640:TTT: 3634/27498) Row 4686998 (NC_000001.11:108774640:TT: 1517/27498)	-	Oct 12, 2022 (156)
71	UK 10K study - Twins Submission ignored due to conflicting rows: Row 1733642 (NC_000001.10:109317263:T: 2034/3708) Row 1733643 (NC_000001.10:109317262:TTT: 1664/3708)	-	Oct 11, 2018 (152)
72	UK 10K study - Twins Submission ignored due to conflicting rows: Row 1733642 (NC_000001.10:109317263:T: 2034/3708) Row 1733643 (NC_000001.10:109317262:TTT: 1664/3708)	-	Oct 11, 2018 (152)
73	ALFA	NC_000001.11 - 108774641	Apr 25, 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)
rs34058938	May 11, 2012 (137)
rs36075191	Oct 16, 2006 (127)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4000147797	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTT:	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTT	(self)
2904737583	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTT	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTT	(self)
2904737583	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
2904737583	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4000147796	NC_000001.11:108774640:TTTTTTTT:	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
2904737583	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4000147795	NC_000001.11:108774640:TTTTTT:	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3687496607, ss4000147794	NC_000001.11:108774640:TTTTT:	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
2904737583	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4000147793, ss5243552159	NC_000001.11:108774640:TTTT:	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
2904737583	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3687496608	NC_000001.11:108774641:TTTT:	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss1701083550, ss1701083719, ss1794905694, ss2987410761, ss5145604980, ss5832460719	NC_000001.10:109317262:TTT:	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3065320846, ss5243552158, ss5444481264, ss5670849893, ss5849061126	NC_000001.11:108774640:TTT:	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
2904737583	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3687496609	NC_000001.11:108774642:TTT:	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3783514679, ss3789157311, ss3794030216, ss5145604982, ss5832460718	NC_000001.10:109317262:TT:	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss1709943971, ss1709943972	NC_000001.10:109317263:TT:	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3065320845, ss5243552157, ss5444481262, ss5670849894	NC_000001.11:108774640:TT:	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
2904737583	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3687496610	NC_000001.11:108774643:TT:	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss41154319	NT_032977.9:79289180:TT:	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss77937236	NC_000001.8:109029324:T:	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss294597632	NC_000001.9:109118805:T:	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
3138773, ss1367811428, ss3794030217, ss5145604981	NC_000001.10:109317262:T:	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
	NC_000001.10:109317263:T:	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3799656031, ss5243552156, ss5444481263, ss5670849892	NC_000001.11:108774640:T:	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
2904737583	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3687496611	NC_000001.11:108774644:T:	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss41154319	NT_032977.9:79289180:TT:T	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss95239894	NT_032977.9:79289200:T:	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4000147787	NC_000001.11:108774640::T	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
2904737583	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4000147788	NC_000001.11:108774640::TT	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
2904737583	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4000147789	NC_000001.11:108774640::TTTT	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
2904737583	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4000147792	NC_000001.11:108774640::TTTTTTTTTT… NC_000001.11:108774640::TTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTCTTTTTTTTT	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4000147790	NC_000001.11:108774640::TTTTTTTT	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
2904737583	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4000147791	NC_000001.11:108774640::TTTTTTTTTT… NC_000001.11:108774640::TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:108774640:TTTTTTTTTTT… NC_000001.11:108774640:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs11290690

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

rs11290690