Name: rs576188809
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.

rs576188809

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:125595842-125595861 (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)₁₂ / del(T)₁₀ / del(T)₈ / de…
del(T)₁₂ / del(T)₁₀ / del(T)₈ / del(T)₆ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₈ / dup(T)₉ / dup(T)₁₀ / dup(T)₁₂ / dup(T)₁₇
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.0994 (923/9282, ALFA)
dupT=0.1589 (796/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: OSBPL11 : 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	9282	TTTTTTTTTTTTTTTTTTTT=0.8790	TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0086, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0994, TTTTTTTTTTTTTTTTTTTTTT=0.0123, TTTTTTTTTTTTTTTTTTTTTTT=0.0006, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.85631	0.048868	0.094822	32
European	Sub	8746	TTTTTTTTTTTTTTTTTTTT=0.8719	TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0091, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.1053, TTTTTTTTTTTTTTTTTTTTTT=0.0129, TTTTTTTTTTTTTTTTTTTTTTT=0.0007, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.847401	0.051979	0.10062	32
African	Sub	158	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	8	TTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	150	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	42	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	32	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	10	TTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	22	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	146	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	38	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	130	TTTTTTTTTTTTTTTTTTTT=0.977	TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.015, TTTTTTTTTTTTTTTTTTTTTT=0.008, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	0.984375	0.0	0.015625	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
Allele Frequency Aggregator	Total	Global	9282	(T)₂₀=0.8790	del(T)₁₂=0.0000, del(T)₁₀=0.0000, del(T)₈=0.0000, del(T)₆=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0086, delT=0.0000, dupT=0.0994, dupTT=0.0123, dupTTT=0.0006, dup(T)₅=0.0000, dup(T)₈=0.0000, dup(T)₉=0.0000
Allele Frequency Aggregator	European	Sub	8746	(T)₂₀=0.8719	del(T)₁₂=0.0000, del(T)₁₀=0.0000, del(T)₈=0.0000, del(T)₆=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0091, delT=0.0000, dupT=0.1053, dupTT=0.0129, dupTTT=0.0007, dup(T)₅=0.0000, dup(T)₈=0.0000, dup(T)₉=0.0000
Allele Frequency Aggregator	African	Sub	158	(T)₂₀=1.000	del(T)₁₂=0.000, del(T)₁₀=0.000, del(T)₈=0.000, del(T)₆=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)₅=0.000, dup(T)₈=0.000, dup(T)₉=0.000
Allele Frequency Aggregator	Latin American 2	Sub	146	(T)₂₀=1.000	del(T)₁₂=0.000, del(T)₁₀=0.000, del(T)₈=0.000, del(T)₆=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)₅=0.000, dup(T)₈=0.000, dup(T)₉=0.000
Allele Frequency Aggregator	Other	Sub	130	(T)₂₀=0.977	del(T)₁₂=0.000, del(T)₁₀=0.000, del(T)₈=0.000, del(T)₆=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.015, dupTT=0.008, dupTTT=0.000, dup(T)₅=0.000, dup(T)₈=0.000, dup(T)₉=0.000
Allele Frequency Aggregator	Asian	Sub	42	(T)₂₀=1.00	del(T)₁₂=0.00, del(T)₁₀=0.00, del(T)₈=0.00, del(T)₆=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)₅=0.00, dup(T)₈=0.00, dup(T)₉=0.00
Allele Frequency Aggregator	South Asian	Sub	38	(T)₂₀=1.00	del(T)₁₂=0.00, del(T)₁₀=0.00, del(T)₈=0.00, del(T)₆=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)₅=0.00, dup(T)₈=0.00, dup(T)₉=0.00
Allele Frequency Aggregator	Latin American 1	Sub	22	(T)₂₀=1.00	del(T)₁₂=0.00, del(T)₁₀=0.00, del(T)₈=0.00, del(T)₆=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)₅=0.00, dup(T)₈=0.00, dup(T)₉=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupT=0.1589
1000Genomes	African	Sub	1322	- No frequency provided	dupT=0.2731
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupT=0.0228
1000Genomes	Europe	Sub	1006	- No frequency provided	dupT=0.2048
1000Genomes	South Asian	Sub	978	- No frequency provided	dupT=0.101
1000Genomes	American	Sub	694	- No frequency provided	dupT=0.154

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 3	NC_000003.12:g.125595850_125595861del
GRCh38.p14 chr 3	NC_000003.12:g.125595852_125595861del
GRCh38.p14 chr 3	NC_000003.12:g.125595854_125595861del
GRCh38.p14 chr 3	NC_000003.12:g.125595856_125595861del
GRCh38.p14 chr 3	NC_000003.12:g.125595858_125595861del
GRCh38.p14 chr 3	NC_000003.12:g.125595859_125595861del
GRCh38.p14 chr 3	NC_000003.12:g.125595860_125595861del
GRCh38.p14 chr 3	NC_000003.12:g.125595861del
GRCh38.p14 chr 3	NC_000003.12:g.125595861dup
GRCh38.p14 chr 3	NC_000003.12:g.125595860_125595861dup
GRCh38.p14 chr 3	NC_000003.12:g.125595859_125595861dup
GRCh38.p14 chr 3	NC_000003.12:g.125595858_125595861dup
GRCh38.p14 chr 3	NC_000003.12:g.125595857_125595861dup
GRCh38.p14 chr 3	NC_000003.12:g.125595854_125595861dup
GRCh38.p14 chr 3	NC_000003.12:g.125595853_125595861dup
GRCh38.p14 chr 3	NC_000003.12:g.125595852_125595861dup
GRCh38.p14 chr 3	NC_000003.12:g.125595850_125595861dup
GRCh38.p14 chr 3	NC_000003.12:g.125595845_125595861dup
GRCh37.p13 chr 3	NC_000003.11:g.125314694_125314705del
GRCh37.p13 chr 3	NC_000003.11:g.125314696_125314705del
GRCh37.p13 chr 3	NC_000003.11:g.125314698_125314705del
GRCh37.p13 chr 3	NC_000003.11:g.125314700_125314705del
GRCh37.p13 chr 3	NC_000003.11:g.125314702_125314705del
GRCh37.p13 chr 3	NC_000003.11:g.125314703_125314705del
GRCh37.p13 chr 3	NC_000003.11:g.125314704_125314705del
GRCh37.p13 chr 3	NC_000003.11:g.125314705del
GRCh37.p13 chr 3	NC_000003.11:g.125314705dup
GRCh37.p13 chr 3	NC_000003.11:g.125314704_125314705dup
GRCh37.p13 chr 3	NC_000003.11:g.125314703_125314705dup
GRCh37.p13 chr 3	NC_000003.11:g.125314702_125314705dup
GRCh37.p13 chr 3	NC_000003.11:g.125314701_125314705dup
GRCh37.p13 chr 3	NC_000003.11:g.125314698_125314705dup
GRCh37.p13 chr 3	NC_000003.11:g.125314697_125314705dup
GRCh37.p13 chr 3	NC_000003.11:g.125314696_125314705dup
GRCh37.p13 chr 3	NC_000003.11:g.125314694_125314705dup
GRCh37.p13 chr 3	NC_000003.11:g.125314689_125314705dup

Gene: OSBPL11, oxysterol binding protein like 11 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
OSBPL11 transcript	NM_022776.5:c.	N/A	Upstream Transcript Variant
OSBPL11 transcript variant X1	XM_047447396.1: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)₂₀=	del(T)₁₂	del(T)₁₀	del(T)₈	del(T)₆	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₈	dup(T)₉	dup(T)₁₀	dup(T)₁₂	dup(T)₁₇
GRCh38.p14 chr 3	NC_000003.12:g.125595842_125595861=	NC_000003.12:g.125595850_125595861del	NC_000003.12:g.125595852_125595861del	NC_000003.12:g.125595854_125595861del	NC_000003.12:g.125595856_125595861del	NC_000003.12:g.125595858_125595861del	NC_000003.12:g.125595859_125595861del	NC_000003.12:g.125595860_125595861del	NC_000003.12:g.125595861del	NC_000003.12:g.125595861dup	NC_000003.12:g.125595860_125595861dup	NC_000003.12:g.125595859_125595861dup	NC_000003.12:g.125595858_125595861dup	NC_000003.12:g.125595857_125595861dup	NC_000003.12:g.125595854_125595861dup	NC_000003.12:g.125595853_125595861dup	NC_000003.12:g.125595852_125595861dup	NC_000003.12:g.125595850_125595861dup	NC_000003.12:g.125595845_125595861dup
GRCh37.p13 chr 3	NC_000003.11:g.125314686_125314705=	NC_000003.11:g.125314694_125314705del	NC_000003.11:g.125314696_125314705del	NC_000003.11:g.125314698_125314705del	NC_000003.11:g.125314700_125314705del	NC_000003.11:g.125314702_125314705del	NC_000003.11:g.125314703_125314705del	NC_000003.11:g.125314704_125314705del	NC_000003.11:g.125314705del	NC_000003.11:g.125314705dup	NC_000003.11:g.125314704_125314705dup	NC_000003.11:g.125314703_125314705dup	NC_000003.11:g.125314702_125314705dup	NC_000003.11:g.125314701_125314705dup	NC_000003.11:g.125314698_125314705dup	NC_000003.11:g.125314697_125314705dup	NC_000003.11:g.125314696_125314705dup	NC_000003.11:g.125314694_125314705dup	NC_000003.11:g.125314689_125314705dup

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#.

47 SubSNP, 29 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41988493	Oct 12, 2018 (152)
2	PJP	ss295123931	Oct 12, 2018 (152)
3	SSMP	ss663352547	Apr 01, 2015 (144)
4	SSIP	ss947096734	Aug 21, 2014 (142)
5	1000GENOMES	ss1370926864	Aug 21, 2014 (142)
6	SWEGEN	ss2993129432	Jan 10, 2018 (151)
7	KHV_HUMAN_GENOMES	ss3803776189	Jul 13, 2019 (153)
8	EVA	ss3828055687	Apr 25, 2020 (154)
9	GNOMAD	ss4080130264	Apr 26, 2021 (155)
10	GNOMAD	ss4080130266	Apr 26, 2021 (155)
11	GNOMAD	ss4080130267	Apr 26, 2021 (155)
12	GNOMAD	ss4080130268	Apr 26, 2021 (155)
13	GNOMAD	ss4080130269	Apr 26, 2021 (155)
14	GNOMAD	ss4080130270	Apr 26, 2021 (155)
15	GNOMAD	ss4080130271	Apr 26, 2021 (155)
16	GNOMAD	ss4080130272	Apr 26, 2021 (155)
17	GNOMAD	ss4080130273	Apr 26, 2021 (155)
18	GNOMAD	ss4080130274	Apr 26, 2021 (155)
19	GNOMAD	ss4080130275	Apr 26, 2021 (155)
20	GNOMAD	ss4080130276	Apr 26, 2021 (155)
21	GNOMAD	ss4080130277	Apr 26, 2021 (155)
22	GNOMAD	ss4080130278	Apr 26, 2021 (155)
23	GNOMAD	ss4080130279	Apr 26, 2021 (155)
24	GNOMAD	ss4080130280	Apr 26, 2021 (155)
25	GNOMAD	ss4080130281	Apr 26, 2021 (155)
26	TOMMO_GENOMICS	ss5161402342	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5161402343	Apr 26, 2021 (155)
28	TOMMO_GENOMICS	ss5161402344	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5161402345	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5161402346	Apr 26, 2021 (155)
31	1000G_HIGH_COVERAGE	ss5255886369	Oct 12, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5255886370	Oct 12, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5255886371	Oct 12, 2022 (156)
34	1000G_HIGH_COVERAGE	ss5255886372	Oct 12, 2022 (156)
35	1000G_HIGH_COVERAGE	ss5255886373	Oct 12, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5255886374	Oct 12, 2022 (156)
37	HUGCELL_USP	ss5455047244	Oct 12, 2022 (156)
38	HUGCELL_USP	ss5455047245	Oct 12, 2022 (156)
39	HUGCELL_USP	ss5455047246	Oct 12, 2022 (156)
40	HUGCELL_USP	ss5455047247	Oct 12, 2022 (156)
41	TOMMO_GENOMICS	ss5694222893	Oct 12, 2022 (156)
42	TOMMO_GENOMICS	ss5694222894	Oct 12, 2022 (156)
43	TOMMO_GENOMICS	ss5694222895	Oct 12, 2022 (156)
44	TOMMO_GENOMICS	ss5694222896	Oct 12, 2022 (156)
45	TOMMO_GENOMICS	ss5694222897	Oct 12, 2022 (156)
46	EVA	ss5826427811	Oct 12, 2022 (156)
47	EVA	ss5826427812	Oct 12, 2022 (156)
48	1000Genomes	NC_000003.11 - 125314686	Oct 12, 2018 (152)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 122657557 (NC_000003.12:125595841::T 48073/103074) Row 122657559 (NC_000003.12:125595841::TT 3579/103080) Row 122657560 (NC_000003.12:125595841::TTT 77/103120)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 122657557 (NC_000003.12:125595841::T 48073/103074) Row 122657559 (NC_000003.12:125595841::TT 3579/103080) Row 122657560 (NC_000003.12:125595841::TTT 77/103120)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 122657557 (NC_000003.12:125595841::T 48073/103074) Row 122657559 (NC_000003.12:125595841::TT 3579/103080) Row 122657560 (NC_000003.12:125595841::TTT 77/103120)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 122657557 (NC_000003.12:125595841::T 48073/103074) Row 122657559 (NC_000003.12:125595841::TT 3579/103080) Row 122657560 (NC_000003.12:125595841::TTT 77/103120)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 122657557 (NC_000003.12:125595841::T 48073/103074) Row 122657559 (NC_000003.12:125595841::TT 3579/103080) Row 122657560 (NC_000003.12:125595841::TTT 77/103120)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 122657557 (NC_000003.12:125595841::T 48073/103074) Row 122657559 (NC_000003.12:125595841::TT 3579/103080) Row 122657560 (NC_000003.12:125595841::TTT 77/103120)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 122657557 (NC_000003.12:125595841::T 48073/103074) Row 122657559 (NC_000003.12:125595841::TT 3579/103080) Row 122657560 (NC_000003.12:125595841::TTT 77/103120)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 122657557 (NC_000003.12:125595841::T 48073/103074) Row 122657559 (NC_000003.12:125595841::TT 3579/103080) Row 122657560 (NC_000003.12:125595841::TTT 77/103120)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 122657557 (NC_000003.12:125595841::T 48073/103074) Row 122657559 (NC_000003.12:125595841::TT 3579/103080) Row 122657560 (NC_000003.12:125595841::TTT 77/103120)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 122657557 (NC_000003.12:125595841::T 48073/103074) Row 122657559 (NC_000003.12:125595841::TT 3579/103080) Row 122657560 (NC_000003.12:125595841::TTT 77/103120)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 122657557 (NC_000003.12:125595841::T 48073/103074) Row 122657559 (NC_000003.12:125595841::TT 3579/103080) Row 122657560 (NC_000003.12:125595841::TTT 77/103120)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 122657557 (NC_000003.12:125595841::T 48073/103074) Row 122657559 (NC_000003.12:125595841::TT 3579/103080) Row 122657560 (NC_000003.12:125595841::TTT 77/103120)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 122657557 (NC_000003.12:125595841::T 48073/103074) Row 122657559 (NC_000003.12:125595841::TT 3579/103080) Row 122657560 (NC_000003.12:125595841::TTT 77/103120)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 122657557 (NC_000003.12:125595841::T 48073/103074) Row 122657559 (NC_000003.12:125595841::TT 3579/103080) Row 122657560 (NC_000003.12:125595841::TTT 77/103120)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 122657557 (NC_000003.12:125595841::T 48073/103074) Row 122657559 (NC_000003.12:125595841::TT 3579/103080) Row 122657560 (NC_000003.12:125595841::TTT 77/103120)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 122657557 (NC_000003.12:125595841::T 48073/103074) Row 122657559 (NC_000003.12:125595841::TT 3579/103080) Row 122657560 (NC_000003.12:125595841::TTT 77/103120)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 122657557 (NC_000003.12:125595841::T 48073/103074) Row 122657559 (NC_000003.12:125595841::TT 3579/103080) Row 122657560 (NC_000003.12:125595841::TTT 77/103120)...	-	Apr 26, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 19371649 (NC_000003.11:125314685:TT: 938/16244) Row 19371650 (NC_000003.11:125314685::TT 1104/16244) Row 19371651 (NC_000003.11:125314685::T 1951/16244)...	-	Apr 26, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 19371649 (NC_000003.11:125314685:TT: 938/16244) Row 19371650 (NC_000003.11:125314685::TT 1104/16244) Row 19371651 (NC_000003.11:125314685::T 1951/16244)...	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 19371649 (NC_000003.11:125314685:TT: 938/16244) Row 19371650 (NC_000003.11:125314685::TT 1104/16244) Row 19371651 (NC_000003.11:125314685::T 1951/16244)...	-	Apr 26, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 19371649 (NC_000003.11:125314685:TT: 938/16244) Row 19371650 (NC_000003.11:125314685::TT 1104/16244) Row 19371651 (NC_000003.11:125314685::T 1951/16244)...	-	Apr 26, 2021 (155)
70	8.3KJPN Submission ignored due to conflicting rows: Row 19371649 (NC_000003.11:125314685:TT: 938/16244) Row 19371650 (NC_000003.11:125314685::TT 1104/16244) Row 19371651 (NC_000003.11:125314685::T 1951/16244)...	-	Apr 26, 2021 (155)
71	14KJPN Submission ignored due to conflicting rows: Row 28059997 (NC_000003.12:125595841::T 3979/28106) Row 28059998 (NC_000003.12:125595841::TT 2256/28106) Row 28059999 (NC_000003.12:125595841:TT: 1951/28106)...	-	Oct 12, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 28059997 (NC_000003.12:125595841::T 3979/28106) Row 28059998 (NC_000003.12:125595841::TT 2256/28106) Row 28059999 (NC_000003.12:125595841:TT: 1951/28106)...	-	Oct 12, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 28059997 (NC_000003.12:125595841::T 3979/28106) Row 28059998 (NC_000003.12:125595841::TT 2256/28106) Row 28059999 (NC_000003.12:125595841:TT: 1951/28106)...	-	Oct 12, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 28059997 (NC_000003.12:125595841::T 3979/28106) Row 28059998 (NC_000003.12:125595841::TT 2256/28106) Row 28059999 (NC_000003.12:125595841:TT: 1951/28106)...	-	Oct 12, 2022 (156)
75	14KJPN Submission ignored due to conflicting rows: Row 28059997 (NC_000003.12:125595841::T 3979/28106) Row 28059998 (NC_000003.12:125595841::TT 2256/28106) Row 28059999 (NC_000003.12:125595841:TT: 1951/28106)...	-	Oct 12, 2022 (156)
76	ALFA	NC_000003.12 - 125595842	Apr 26, 2021 (155)

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

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
4065703159	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTT	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTT	(self)
ss4080130281	NC_000003.12:125595841:TTTTTTTTTT:	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
4065703159	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss5161402346	NC_000003.11:125314685:TTTTTTTT:	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4080130280, ss5694222897	NC_000003.12:125595841:TTTTTTTT:	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
4065703159	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4080130279	NC_000003.12:125595841:TTTTTT:	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
4065703159	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4080130278	NC_000003.12:125595841:TTTT:	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
4065703159	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4080130277	NC_000003.12:125595841:TTT:	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
4065703159	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss2993129432, ss5161402342	NC_000003.11:125314685:TT:	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4080130276, ss5255886370, ss5455047246, ss5694222895	NC_000003.12:125595841:TT:	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
4065703159	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss5161402345	NC_000003.11:125314685:T:	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4080130275, ss5255886372, ss5455047244, ss5694222896	NC_000003.12:125595841:T:	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
4065703159	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss295123931	NC_000003.10:126797395::T	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
17251852, ss663352547, ss1370926864, ss3828055687, ss5161402344, ss5826427811	NC_000003.11:125314685::T	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3803776189, ss4080130264, ss5255886371, ss5455047245, ss5694222893	NC_000003.12:125595841::T	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
4065703159	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss41988493	NT_005612.16:31809831::T	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss947096734, ss5161402343	NC_000003.11:125314685::TT	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4080130266, ss5255886369, ss5455047247, ss5694222894	NC_000003.12:125595841::TT	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
4065703159	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss5826427812	NC_000003.11:125314685::TTT	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT
ss4080130267, ss5255886373	NC_000003.12:125595841::TTT	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
4065703159	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4080130268	NC_000003.12:125595841::TTTT	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4080130269	NC_000003.12:125595841::TTTTT	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4065703159	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4080130270, ss5255886374	NC_000003.12:125595841::TTTTTTTT	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4065703159	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4080130271	NC_000003.12:125595841::TTTTTTTTT	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4065703159	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4080130272	NC_000003.12:125595841::TTTTTTTTTT	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4080130273	NC_000003.12:125595841::TTTTTTTTTT… NC_000003.12:125595841::TTTTTTTTTTTT	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4080130274	NC_000003.12:125595841::TTTTTTTTTT… NC_000003.12:125595841::TTTTTTTTTTTTTTTTT	NC_000003.12:125595841:TTTTTTTTTTT… NC_000003.12:125595841:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs576188809

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

rs576188809