Name: rs71008267
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.

rs71008267

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:183126643-183126653 (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: delTTT / delTT / delT / dupT / dup…
delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / ins(T)₂₉
Variation Type: Indel Insertion and Deletion
Frequency: delT=0.3638 (1822/5008, 1000G)
delTTT=0.0000 (0/2852, ALFA)
delTT=0.0000 (0/2852, ALFA) (+ 6 more)
delT=0.0000 (0/2852, ALFA)
dupT=0.0000 (0/2852, ALFA)
dupTT=0.0000 (0/2852, ALFA)
dupTTT=0.0000 (0/2852, ALFA)
dup(T)₄=0.0000 (0/2852, ALFA)
dup(T)₅=0.0000 (0/2852, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NUP35 : Intron Variant
LOC124907917 : 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	HWEP
Total	Global	2852	TTTTTTTTTTT=1.0000	TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000	1.0	N/A
European	Sub	2098	TTTTTTTTTTT=1.0000	TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	272	TTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000	1.0	N/A
African Others	Sub	4	TTTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0	1.0	N/A
African American	Sub	268	TTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000	1.0	N/A
Asian	Sub	52	TTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	N/A
East Asian	Sub	38	TTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	14	TTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 1	Sub	52	TTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 2	Sub	222	TTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	26	TTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	130	TTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000	1.0	N/A

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

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
1000Genomes	Global	Study-wide	5008	(T)₁₁=0.6362	delT=0.3638
1000Genomes	African	Sub	1322	(T)₁₁=0.2905	delT=0.7095
1000Genomes	East Asian	Sub	1008	(T)₁₁=0.8661	delT=0.1339
1000Genomes	Europe	Sub	1006	(T)₁₁=0.6600	delT=0.3400
1000Genomes	South Asian	Sub	978	(T)₁₁=0.770	delT=0.230
1000Genomes	American	Sub	694	(T)₁₁=0.738	delT=0.262
Allele Frequency Aggregator	Total	Global	2852	(T)₁₁=1.0000	delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0000
Allele Frequency Aggregator	European	Sub	2098	(T)₁₁=1.0000	delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0000
Allele Frequency Aggregator	African	Sub	272	(T)₁₁=1.000	delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000
Allele Frequency Aggregator	Latin American 2	Sub	222	(T)₁₁=1.000	delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000
Allele Frequency Aggregator	Other	Sub	130	(T)₁₁=1.000	delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000
Allele Frequency Aggregator	Latin American 1	Sub	52	(T)₁₁=1.00	delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00
Allele Frequency Aggregator	Asian	Sub	52	(T)₁₁=1.00	delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	26	(T)₁₁=1.00	delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=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 2	NC_000002.12:g.183126651_183126653del
GRCh38.p14 chr 2	NC_000002.12:g.183126652_183126653del
GRCh38.p14 chr 2	NC_000002.12:g.183126653del
GRCh38.p14 chr 2	NC_000002.12:g.183126653dup
GRCh38.p14 chr 2	NC_000002.12:g.183126652_183126653dup
GRCh38.p14 chr 2	NC_000002.12:g.183126651_183126653dup
GRCh38.p14 chr 2	NC_000002.12:g.183126650_183126653dup
GRCh38.p14 chr 2	NC_000002.12:g.183126649_183126653dup
GRCh38.p14 chr 2	NC_000002.12:g.183126648_183126653dup
GRCh38.p14 chr 2	NC_000002.12:g.183126653_183126654insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 2	NC_000002.11:g.183991379_183991381del
GRCh37.p13 chr 2	NC_000002.11:g.183991380_183991381del
GRCh37.p13 chr 2	NC_000002.11:g.183991381del
GRCh37.p13 chr 2	NC_000002.11:g.183991381dup
GRCh37.p13 chr 2	NC_000002.11:g.183991380_183991381dup
GRCh37.p13 chr 2	NC_000002.11:g.183991379_183991381dup
GRCh37.p13 chr 2	NC_000002.11:g.183991378_183991381dup
GRCh37.p13 chr 2	NC_000002.11:g.183991377_183991381dup
GRCh37.p13 chr 2	NC_000002.11:g.183991376_183991381dup
GRCh37.p13 chr 2	NC_000002.11:g.183991381_183991382insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: NUP35, nucleoporin 35 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NUP35 transcript variant 3	NM_001287584.2:c.-11-1636… NM_001287584.2:c.-11-1636_-11-1634del	N/A	Intron Variant
NUP35 transcript variant 4	NM_001287585.2:c.-437-163… NM_001287585.2:c.-437-1636_-437-1634del	N/A	Intron Variant
NUP35 transcript variant 1	NM_138285.5:c.41-1636_41-… NM_138285.5:c.41-1636_41-1634del	N/A	Intron Variant
NUP35 transcript variant 2	NR_109856.2:n.	N/A	Intron Variant
NUP35 transcript variant X2	XM_006712254.4:c.-11-1636… XM_006712254.4:c.-11-1636_-11-1634del	N/A	Intron Variant
NUP35 transcript variant X5	XM_011510576.4:c.-11-1636… XM_011510576.4:c.-11-1636_-11-1634del	N/A	Intron Variant
NUP35 transcript variant X3	XM_011510577.3:c.-11-1636… XM_011510577.3:c.-11-1636_-11-1634del	N/A	Intron Variant
NUP35 transcript variant X1	XM_017003308.1:c.50-1636_… XM_017003308.1:c.50-1636_50-1634del	N/A	Intron Variant
NUP35 transcript variant X4	XM_047443270.1:c.-11-1636… XM_047443270.1:c.-11-1636_-11-1634del	N/A	Intron Variant

Gene: LOC124907917, uncharacterized LOC124907917 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
LOC124907917 transcript	XR_007087331.1:n.	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)₁₁=	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	ins(T)₂₉
GRCh38.p14 chr 2	NC_000002.12:g.183126643_183126653=	NC_000002.12:g.183126651_183126653del	NC_000002.12:g.183126652_183126653del	NC_000002.12:g.183126653del	NC_000002.12:g.183126653dup	NC_000002.12:g.183126652_183126653dup	NC_000002.12:g.183126651_183126653dup	NC_000002.12:g.183126650_183126653dup	NC_000002.12:g.183126649_183126653dup	NC_000002.12:g.183126648_183126653dup	NC_000002.12:g.183126653_183126654insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 2	NC_000002.11:g.183991371_183991381=	NC_000002.11:g.183991379_183991381del	NC_000002.11:g.183991380_183991381del	NC_000002.11:g.183991381del	NC_000002.11:g.183991381dup	NC_000002.11:g.183991380_183991381dup	NC_000002.11:g.183991379_183991381dup	NC_000002.11:g.183991378_183991381dup	NC_000002.11:g.183991377_183991381dup	NC_000002.11:g.183991376_183991381dup	NC_000002.11:g.183991381_183991382insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NUP35 transcript variant 3	NM_001287584.2:c.-11-1644=	NM_001287584.2:c.-11-1636_-11-1634del	NM_001287584.2:c.-11-1635_-11-1634del	NM_001287584.2:c.-11-1634del	NM_001287584.2:c.-11-1634dup	NM_001287584.2:c.-11-1635_-11-1634dup	NM_001287584.2:c.-11-1636_-11-1634dup	NM_001287584.2:c.-11-1637_-11-1634dup	NM_001287584.2:c.-11-1638_-11-1634dup	NM_001287584.2:c.-11-1639_-11-1634dup	NM_001287584.2:c.-11-1634_-11-1633insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NUP35 transcript variant 4	NM_001287585.2:c.-437-1644=	NM_001287585.2:c.-437-1636_-437-1634del	NM_001287585.2:c.-437-1635_-437-1634del	NM_001287585.2:c.-437-1634del	NM_001287585.2:c.-437-1634dup	NM_001287585.2:c.-437-1635_-437-1634dup	NM_001287585.2:c.-437-1636_-437-1634dup	NM_001287585.2:c.-437-1637_-437-1634dup	NM_001287585.2:c.-437-1638_-437-1634dup	NM_001287585.2:c.-437-1639_-437-1634dup	NM_001287585.2:c.-437-1634_-437-1633insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NUP35 transcript	NM_138285.3:c.41-1644=	NM_138285.3:c.41-1636_41-1634del	NM_138285.3:c.41-1635_41-1634del	NM_138285.3:c.41-1634del	NM_138285.3:c.41-1634dup	NM_138285.3:c.41-1635_41-1634dup	NM_138285.3:c.41-1636_41-1634dup	NM_138285.3:c.41-1637_41-1634dup	NM_138285.3:c.41-1638_41-1634dup	NM_138285.3:c.41-1639_41-1634dup	NM_138285.3:c.41-1634_41-1633insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NUP35 transcript variant 1	NM_138285.5:c.41-1644=	NM_138285.5:c.41-1636_41-1634del	NM_138285.5:c.41-1635_41-1634del	NM_138285.5:c.41-1634del	NM_138285.5:c.41-1634dup	NM_138285.5:c.41-1635_41-1634dup	NM_138285.5:c.41-1636_41-1634dup	NM_138285.5:c.41-1637_41-1634dup	NM_138285.5:c.41-1638_41-1634dup	NM_138285.5:c.41-1639_41-1634dup	NM_138285.5:c.41-1634_41-1633insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NUP35 transcript variant X1	XM_005246284.1:c.50-1644=	XM_005246284.1:c.50-1636_50-1634del	XM_005246284.1:c.50-1635_50-1634del	XM_005246284.1:c.50-1634del	XM_005246284.1:c.50-1634dup	XM_005246284.1:c.50-1635_50-1634dup	XM_005246284.1:c.50-1636_50-1634dup	XM_005246284.1:c.50-1637_50-1634dup	XM_005246284.1:c.50-1638_50-1634dup	XM_005246284.1:c.50-1639_50-1634dup	XM_005246284.1:c.50-1634_50-1633insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NUP35 transcript variant X2	XM_005246285.1:c.-11-1644=	XM_005246285.1:c.-11-1636_-11-1634del	XM_005246285.1:c.-11-1635_-11-1634del	XM_005246285.1:c.-11-1634del	XM_005246285.1:c.-11-1634dup	XM_005246285.1:c.-11-1635_-11-1634dup	XM_005246285.1:c.-11-1636_-11-1634dup	XM_005246285.1:c.-11-1637_-11-1634dup	XM_005246285.1:c.-11-1638_-11-1634dup	XM_005246285.1:c.-11-1639_-11-1634dup	XM_005246285.1:c.-11-1634_-11-1633insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NUP35 transcript variant X3	XM_005246286.1:c.-437-1644=	XM_005246286.1:c.-437-1636_-437-1634del	XM_005246286.1:c.-437-1635_-437-1634del	XM_005246286.1:c.-437-1634del	XM_005246286.1:c.-437-1634dup	XM_005246286.1:c.-437-1635_-437-1634dup	XM_005246286.1:c.-437-1636_-437-1634dup	XM_005246286.1:c.-437-1637_-437-1634dup	XM_005246286.1:c.-437-1638_-437-1634dup	XM_005246286.1:c.-437-1639_-437-1634dup	XM_005246286.1:c.-437-1634_-437-1633insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NUP35 transcript variant X2	XM_006712254.4:c.-11-1644=	XM_006712254.4:c.-11-1636_-11-1634del	XM_006712254.4:c.-11-1635_-11-1634del	XM_006712254.4:c.-11-1634del	XM_006712254.4:c.-11-1634dup	XM_006712254.4:c.-11-1635_-11-1634dup	XM_006712254.4:c.-11-1636_-11-1634dup	XM_006712254.4:c.-11-1637_-11-1634dup	XM_006712254.4:c.-11-1638_-11-1634dup	XM_006712254.4:c.-11-1639_-11-1634dup	XM_006712254.4:c.-11-1634_-11-1633insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NUP35 transcript variant X5	XM_011510576.4:c.-11-1644=	XM_011510576.4:c.-11-1636_-11-1634del	XM_011510576.4:c.-11-1635_-11-1634del	XM_011510576.4:c.-11-1634del	XM_011510576.4:c.-11-1634dup	XM_011510576.4:c.-11-1635_-11-1634dup	XM_011510576.4:c.-11-1636_-11-1634dup	XM_011510576.4:c.-11-1637_-11-1634dup	XM_011510576.4:c.-11-1638_-11-1634dup	XM_011510576.4:c.-11-1639_-11-1634dup	XM_011510576.4:c.-11-1634_-11-1633insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NUP35 transcript variant X3	XM_011510577.3:c.-11-1644=	XM_011510577.3:c.-11-1636_-11-1634del	XM_011510577.3:c.-11-1635_-11-1634del	XM_011510577.3:c.-11-1634del	XM_011510577.3:c.-11-1634dup	XM_011510577.3:c.-11-1635_-11-1634dup	XM_011510577.3:c.-11-1636_-11-1634dup	XM_011510577.3:c.-11-1637_-11-1634dup	XM_011510577.3:c.-11-1638_-11-1634dup	XM_011510577.3:c.-11-1639_-11-1634dup	XM_011510577.3:c.-11-1634_-11-1633insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NUP35 transcript variant X1	XM_017003308.1:c.50-1644=	XM_017003308.1:c.50-1636_50-1634del	XM_017003308.1:c.50-1635_50-1634del	XM_017003308.1:c.50-1634del	XM_017003308.1:c.50-1634dup	XM_017003308.1:c.50-1635_50-1634dup	XM_017003308.1:c.50-1636_50-1634dup	XM_017003308.1:c.50-1637_50-1634dup	XM_017003308.1:c.50-1638_50-1634dup	XM_017003308.1:c.50-1639_50-1634dup	XM_017003308.1:c.50-1634_50-1633insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NUP35 transcript variant X4	XM_047443270.1:c.-11-1644=	XM_047443270.1:c.-11-1636_-11-1634del	XM_047443270.1:c.-11-1635_-11-1634del	XM_047443270.1:c.-11-1634del	XM_047443270.1:c.-11-1634dup	XM_047443270.1:c.-11-1635_-11-1634dup	XM_047443270.1:c.-11-1636_-11-1634dup	XM_047443270.1:c.-11-1637_-11-1634dup	XM_047443270.1:c.-11-1638_-11-1634dup	XM_047443270.1:c.-11-1639_-11-1634dup	XM_047443270.1:c.-11-1634_-11-1633insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

65 SubSNP, 33 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95295455	Feb 13, 2009 (130)
2	GMI	ss288263553	May 04, 2012 (137)
3	SSMP	ss663265410	Apr 01, 2015 (144)
4	BILGI_BIOE	ss666178754	Apr 25, 2013 (138)
5	1000GENOMES	ss1369286550	Aug 21, 2014 (142)
6	EVA_UK10K_ALSPAC	ss1703314658	Apr 01, 2015 (144)
7	EVA_UK10K_TWINSUK	ss1703314665	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1710042203	Apr 01, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1710042229	Apr 01, 2015 (144)
10	HAMMER_LAB	ss1798035818	Sep 08, 2015 (146)
11	SWEGEN	ss2990996841	Nov 08, 2017 (151)
12	BIOINF_KMB_FNS_UNIBA	ss3645600400	Oct 11, 2018 (152)
13	URBANLAB	ss3647225120	Oct 11, 2018 (152)
14	EVA_DECODE	ss3705581947	Jul 13, 2019 (153)
15	EVA_DECODE	ss3705581948	Jul 13, 2019 (153)
16	EVA_DECODE	ss3705581949	Jul 13, 2019 (153)
17	EVA_DECODE	ss3705581950	Jul 13, 2019 (153)
18	ACPOP	ss3729179124	Jul 13, 2019 (153)
19	ACPOP	ss3729179125	Jul 13, 2019 (153)
20	ACPOP	ss3729179126	Jul 13, 2019 (153)
21	ACPOP	ss3729179127	Jul 13, 2019 (153)
22	INMEGENXS	ss3745641152	Jul 13, 2019 (153)
23	PACBIO	ss3784089155	Jul 13, 2019 (153)
24	PACBIO	ss3789637327	Jul 13, 2019 (153)
25	PACBIO	ss3794510442	Jul 13, 2019 (153)
26	KHV_HUMAN_GENOMES	ss3802175194	Jul 13, 2019 (153)
27	EVA	ss3827394487	Apr 25, 2020 (154)
28	EVA	ss3837116148	Apr 25, 2020 (154)
29	EVA	ss3842536564	Apr 25, 2020 (154)
30	KOGIC	ss3949652973	Apr 25, 2020 (154)
31	KOGIC	ss3949652974	Apr 25, 2020 (154)
32	KOGIC	ss3949652975	Apr 25, 2020 (154)
33	KOGIC	ss3949652976	Apr 25, 2020 (154)
34	GNOMAD	ss4057016371	Apr 26, 2021 (155)
35	GNOMAD	ss4057016372	Apr 26, 2021 (155)
36	GNOMAD	ss4057016373	Apr 26, 2021 (155)
37	GNOMAD	ss4057016374	Apr 26, 2021 (155)
38	GNOMAD	ss4057016375	Apr 26, 2021 (155)
39	GNOMAD	ss4057016376	Apr 26, 2021 (155)
40	GNOMAD	ss4057016377	Apr 26, 2021 (155)
41	GNOMAD	ss4057016378	Apr 26, 2021 (155)
42	GNOMAD	ss4057016379	Apr 26, 2021 (155)
43	GNOMAD	ss4057016380	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5155475433	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5155475434	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5155475435	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5155475436	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5155475437	Apr 26, 2021 (155)
49	1000G_HIGH_COVERAGE	ss5251243601	Oct 12, 2022 (156)
50	1000G_HIGH_COVERAGE	ss5251243602	Oct 12, 2022 (156)
51	1000G_HIGH_COVERAGE	ss5251243603	Oct 12, 2022 (156)
52	1000G_HIGH_COVERAGE	ss5251243604	Oct 12, 2022 (156)
53	1000G_HIGH_COVERAGE	ss5251243605	Oct 12, 2022 (156)
54	1000G_HIGH_COVERAGE	ss5251243606	Oct 12, 2022 (156)
55	HUGCELL_USP	ss5450940104	Oct 12, 2022 (156)
56	HUGCELL_USP	ss5450940105	Oct 12, 2022 (156)
57	HUGCELL_USP	ss5450940106	Oct 12, 2022 (156)
58	HUGCELL_USP	ss5450940107	Oct 12, 2022 (156)
59	HUGCELL_USP	ss5450940108	Oct 12, 2022 (156)
60	TOMMO_GENOMICS	ss5686061900	Oct 12, 2022 (156)
61	TOMMO_GENOMICS	ss5686061901	Oct 12, 2022 (156)
62	TOMMO_GENOMICS	ss5686061902	Oct 12, 2022 (156)
63	TOMMO_GENOMICS	ss5686061904	Oct 12, 2022 (156)
64	EVA	ss5821289070	Oct 12, 2022 (156)
65	EVA	ss5821289071	Oct 12, 2022 (156)
66	1000Genomes	NC_000002.11 - 183991371	Oct 11, 2018 (152)
67	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 6527982 (NC_000002.11:183991370:T: 1465/3854) Row 6527983 (NC_000002.11:183991370::TTTT 308/3854)	-	Oct 11, 2018 (152)
68	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 6527982 (NC_000002.11:183991370:T: 1465/3854) Row 6527983 (NC_000002.11:183991370::TTTT 308/3854)	-	Oct 11, 2018 (152)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 84188585 (NC_000002.12:183126642::T 493/134140) Row 84188586 (NC_000002.12:183126642::TT 4338/134176) Row 84188587 (NC_000002.12:183126642::TTT 2008/134160)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 84188585 (NC_000002.12:183126642::T 493/134140) Row 84188586 (NC_000002.12:183126642::TT 4338/134176) Row 84188587 (NC_000002.12:183126642::TTT 2008/134160)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 84188585 (NC_000002.12:183126642::T 493/134140) Row 84188586 (NC_000002.12:183126642::TT 4338/134176) Row 84188587 (NC_000002.12:183126642::TTT 2008/134160)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 84188585 (NC_000002.12:183126642::T 493/134140) Row 84188586 (NC_000002.12:183126642::TT 4338/134176) Row 84188587 (NC_000002.12:183126642::TTT 2008/134160)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 84188585 (NC_000002.12:183126642::T 493/134140) Row 84188586 (NC_000002.12:183126642::TT 4338/134176) Row 84188587 (NC_000002.12:183126642::TTT 2008/134160)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 84188585 (NC_000002.12:183126642::T 493/134140) Row 84188586 (NC_000002.12:183126642::TT 4338/134176) Row 84188587 (NC_000002.12:183126642::TTT 2008/134160)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 84188585 (NC_000002.12:183126642::T 493/134140) Row 84188586 (NC_000002.12:183126642::TT 4338/134176) Row 84188587 (NC_000002.12:183126642::TTT 2008/134160)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 84188585 (NC_000002.12:183126642::T 493/134140) Row 84188586 (NC_000002.12:183126642::TT 4338/134176) Row 84188587 (NC_000002.12:183126642::TTT 2008/134160)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 84188585 (NC_000002.12:183126642::T 493/134140) Row 84188586 (NC_000002.12:183126642::TT 4338/134176) Row 84188587 (NC_000002.12:183126642::TTT 2008/134160)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 84188585 (NC_000002.12:183126642::T 493/134140) Row 84188586 (NC_000002.12:183126642::TT 4338/134176) Row 84188587 (NC_000002.12:183126642::TTT 2008/134160)...	-	Apr 26, 2021 (155)
79	Korean Genome Project Submission ignored due to conflicting rows: Row 6030974 (NC_000002.12:183126642:T: 291/1828) Row 6030975 (NC_000002.12:183126643::T 101/1828) Row 6030976 (NC_000002.12:183126643::TTTT 162/1828)...	-	Apr 25, 2020 (154)
80	Korean Genome Project Submission ignored due to conflicting rows: Row 6030974 (NC_000002.12:183126642:T: 291/1828) Row 6030975 (NC_000002.12:183126643::T 101/1828) Row 6030976 (NC_000002.12:183126643::TTTT 162/1828)...	-	Apr 25, 2020 (154)
81	Korean Genome Project Submission ignored due to conflicting rows: Row 6030974 (NC_000002.12:183126642:T: 291/1828) Row 6030975 (NC_000002.12:183126643::T 101/1828) Row 6030976 (NC_000002.12:183126643::TTTT 162/1828)...	-	Apr 25, 2020 (154)
82	Korean Genome Project Submission ignored due to conflicting rows: Row 6030974 (NC_000002.12:183126642:T: 291/1828) Row 6030975 (NC_000002.12:183126643::T 101/1828) Row 6030976 (NC_000002.12:183126643::TTTT 162/1828)...	-	Apr 25, 2020 (154)
83	Northern Sweden Submission ignored due to conflicting rows: Row 2463989 (NC_000002.11:183991370:T: 220/600) Row 2463990 (NC_000002.11:183991370::TTT 4/600) Row 2463991 (NC_000002.11:183991370::TTTT 19/600)...	-	Jul 13, 2019 (153)
84	Northern Sweden Submission ignored due to conflicting rows: Row 2463989 (NC_000002.11:183991370:T: 220/600) Row 2463990 (NC_000002.11:183991370::TTT 4/600) Row 2463991 (NC_000002.11:183991370::TTTT 19/600)...	-	Jul 13, 2019 (153)
85	Northern Sweden Submission ignored due to conflicting rows: Row 2463989 (NC_000002.11:183991370:T: 220/600) Row 2463990 (NC_000002.11:183991370::TTT 4/600) Row 2463991 (NC_000002.11:183991370::TTTT 19/600)...	-	Jul 13, 2019 (153)
86	Northern Sweden Submission ignored due to conflicting rows: Row 2463989 (NC_000002.11:183991370:T: 220/600) Row 2463990 (NC_000002.11:183991370::TTT 4/600) Row 2463991 (NC_000002.11:183991370::TTTT 19/600)...	-	Jul 13, 2019 (153)
87	8.3KJPN Submission ignored due to conflicting rows: Row 13444740 (NC_000002.11:183991370::TTTT 1304/16756) Row 13444741 (NC_000002.11:183991370:T: 2628/16756) Row 13444742 (NC_000002.11:183991370::T 864/16756)...	-	Apr 26, 2021 (155)
88	8.3KJPN Submission ignored due to conflicting rows: Row 13444740 (NC_000002.11:183991370::TTTT 1304/16756) Row 13444741 (NC_000002.11:183991370:T: 2628/16756) Row 13444742 (NC_000002.11:183991370::T 864/16756)...	-	Apr 26, 2021 (155)
89	8.3KJPN Submission ignored due to conflicting rows: Row 13444740 (NC_000002.11:183991370::TTTT 1304/16756) Row 13444741 (NC_000002.11:183991370:T: 2628/16756) Row 13444742 (NC_000002.11:183991370::T 864/16756)...	-	Apr 26, 2021 (155)
90	8.3KJPN Submission ignored due to conflicting rows: Row 13444740 (NC_000002.11:183991370::TTTT 1304/16756) Row 13444741 (NC_000002.11:183991370:T: 2628/16756) Row 13444742 (NC_000002.11:183991370::T 864/16756)...	-	Apr 26, 2021 (155)
91	8.3KJPN Submission ignored due to conflicting rows: Row 13444740 (NC_000002.11:183991370::TTTT 1304/16756) Row 13444741 (NC_000002.11:183991370:T: 2628/16756) Row 13444742 (NC_000002.11:183991370::T 864/16756)...	-	Apr 26, 2021 (155)
92	14KJPN Submission ignored due to conflicting rows: Row 19899004 (NC_000002.12:183126642:T: 4435/28256) Row 19899005 (NC_000002.12:183126642::T 1451/28256) Row 19899006 (NC_000002.12:183126642::TTTT 2189/28256)...	-	Oct 12, 2022 (156)
93	14KJPN Submission ignored due to conflicting rows: Row 19899004 (NC_000002.12:183126642:T: 4435/28256) Row 19899005 (NC_000002.12:183126642::T 1451/28256) Row 19899006 (NC_000002.12:183126642::TTTT 2189/28256)...	-	Oct 12, 2022 (156)
94	14KJPN Submission ignored due to conflicting rows: Row 19899004 (NC_000002.12:183126642:T: 4435/28256) Row 19899005 (NC_000002.12:183126642::T 1451/28256) Row 19899006 (NC_000002.12:183126642::TTTT 2189/28256)...	-	Oct 12, 2022 (156)
95	14KJPN Submission ignored due to conflicting rows: Row 19899004 (NC_000002.12:183126642:T: 4435/28256) Row 19899005 (NC_000002.12:183126642::T 1451/28256) Row 19899006 (NC_000002.12:183126642::TTTT 2189/28256)...	-	Oct 12, 2022 (156)
96	UK 10K study - Twins Submission ignored due to conflicting rows: Row 6527982 (NC_000002.11:183991370:T: 1452/3708) Row 6527983 (NC_000002.11:183991370::TTTT 277/3708)	-	Oct 11, 2018 (152)
97	UK 10K study - Twins Submission ignored due to conflicting rows: Row 6527982 (NC_000002.11:183991370:T: 1452/3708) Row 6527983 (NC_000002.11:183991370::TTTT 277/3708)	-	Oct 11, 2018 (152)
98	ALFA	NC_000002.12 - 183126643	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)
rs72257874	May 11, 2012 (137)
rs369471095	May 13, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4057016380	NC_000002.12:183126642:TTT:	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTT	(self)
1893559042	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTT	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTT	(self)
ss5155475437	NC_000002.11:183991370:TT:	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTT	(self)
ss4057016379	NC_000002.12:183126642:TT:	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTT	(self)
1893559042	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTT	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTT	(self)
ss288263553	NC_000002.10:183699615:T:	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTT	(self)
11813908, ss666178754, ss1369286550, ss1703314658, ss1703314665, ss1798035818, ss2990996841, ss3729179124, ss3784089155, ss3789637327, ss3794510442, ss3827394487, ss5155475434, ss5821289070	NC_000002.11:183991370:T:	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTT	(self)
ss3645600400, ss3647225120, ss3705581947, ss3802175194, ss3949652973, ss4057016378, ss5251243603, ss5450940104, ss5686061900	NC_000002.12:183126642:T:	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTT	(self)
1893559042	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTT	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTT	(self)
ss95295455	NT_005403.17:34200798:T:	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTT	(self)
ss5155475435	NC_000002.11:183991370::T	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4057016371, ss5251243601, ss5450940105, ss5686061901	NC_000002.12:183126642::T	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTTTT	(self)
1893559042	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTTTT	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3949652974	NC_000002.12:183126643::T	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3729179127, ss3837116148	NC_000002.11:183991370::TT	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3842536564, ss4057016372, ss5251243604, ss5450940106	NC_000002.12:183126642::TT	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTTTTT	(self)
1893559042	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTTTTT	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3705581948	NC_000002.12:183126643::TT	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3729179125, ss5155475436	NC_000002.11:183991370::TTT	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4057016373, ss5251243605, ss5450940108, ss5686061904	NC_000002.12:183126642::TTT	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
1893559042	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3705581949	NC_000002.12:183126643::TTT	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss663265410, ss3729179126, ss3745641152, ss5155475433, ss5821289071	NC_000002.11:183991370::TTTT	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss1710042203, ss1710042229	NC_000002.11:183991371::TTTT	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4057016374, ss5251243602, ss5450940107, ss5686061902	NC_000002.12:183126642::TTTT	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
1893559042	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3705581950, ss3949652975	NC_000002.12:183126643::TTTT	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4057016375, ss5251243606	NC_000002.12:183126642::TTTTT	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
1893559042	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3949652976	NC_000002.12:183126643::TTTTT	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4057016376	NC_000002.12:183126642::TTTTTT	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4057016377	NC_000002.12:183126642::TTTTTTTTTT… NC_000002.12:183126642::TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:183126642:TTTTTTTTTTT… NC_000002.12:183126642:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

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

No publications for rs71008267

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

rs71008267