Name: rs1482062110
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.

rs1482062110

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr9:121287081 (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: C>A / C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.00000 (0/14048, ALFA)
T=0.00000 (0/14048, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: GSN : Intron Variant
GSN-AS1 : 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	14048	C=1.00000	A=0.00000, T=0.00000	1.0	N/A
European	Sub	9688	C=1.0000	A=0.0000, T=0.0000	1.0	N/A
African	Sub	2898	C=1.0000	A=0.0000, T=0.0000	1.0	N/A
African Others	Sub	114	C=1.000	A=0.000, T=0.000	1.0	N/A
African American	Sub	2784	C=1.0000	A=0.0000, T=0.0000	1.0	N/A
Asian	Sub	112	C=1.000	A=0.000, T=0.000	1.0	N/A
East Asian	Sub	86	C=1.00	A=0.00, T=0.00	1.0	N/A
Other Asian	Sub	26	C=1.00	A=0.00, T=0.00	1.0	N/A
Latin American 1	Sub	146	C=1.000	A=0.000, T=0.000	1.0	N/A
Latin American 2	Sub	610	C=1.000	A=0.000, T=0.000	1.0	N/A
South Asian	Sub	98	C=1.00	A=0.00, T=0.00	1.0	N/A
Other	Sub	496	C=1.000	A=0.000, T=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
Allele Frequency Aggregator	Total	Global	14048	C=1.00000	A=0.00000, T=0.00000
Allele Frequency Aggregator	European	Sub	9688	C=1.0000	A=0.0000, T=0.0000
Allele Frequency Aggregator	African	Sub	2898	C=1.0000	A=0.0000, T=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	610	C=1.000	A=0.000, T=0.000
Allele Frequency Aggregator	Other	Sub	496	C=1.000	A=0.000, T=0.000
Allele Frequency Aggregator	Latin American 1	Sub	146	C=1.000	A=0.000, T=0.000
Allele Frequency Aggregator	Asian	Sub	112	C=1.000	A=0.000, T=0.000
Allele Frequency Aggregator	South Asian	Sub	98	C=1.00	A=0.00, T=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 9	NC_000009.12:g.121287081C>A
GRCh38.p14 chr 9	NC_000009.12:g.121287081C>T
GRCh37.p13 chr 9	NC_000009.11:g.124049359C>A
GRCh37.p13 chr 9	NC_000009.11:g.124049359C>T
GSN RefSeqGene	NG_012872.2:g.91000C>A
GSN RefSeqGene	NG_012872.2:g.91000C>T

Gene: GSN, gelsolin (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
GSN transcript variant 3	NM_001127662.2:c.-9-14882… NM_001127662.2:c.-9-14882C>A	N/A	Intron Variant
GSN transcript variant 4	NM_001127663.2:c.99+4531C… NM_001127663.2:c.99+4531C>A	N/A	Intron Variant
GSN transcript variant 5	NM_001127664.2:c.-10+5128… NM_001127664.2:c.-10+5128C>A	N/A	Intron Variant
GSN transcript variant 6	NM_001127665.2:c.-10+3689… NM_001127665.2:c.-10+3689C>A	N/A	Intron Variant
GSN transcript variant 7	NM_001127666.2:c.-48+5519… NM_001127666.2:c.-48+5519C>A	N/A	Intron Variant
GSN transcript variant 8	NM_001127667.2:c.-39+5519… NM_001127667.2:c.-39+5519C>A	N/A	Intron Variant
GSN transcript variant 9	NM_001258029.2:c.42+896C>A	N/A	Intron Variant
GSN transcript variant 10	NM_001258030.2:c.15+320C>A	N/A	Intron Variant
GSN transcript variant 11	NM_001353053.1:c.-10+5519… NM_001353053.1:c.-10+5519C>A	N/A	Intron Variant
GSN transcript variant 12	NM_001353054.1:c.-10+5519… NM_001353054.1:c.-10+5519C>A	N/A	Intron Variant
GSN transcript variant 13	NM_001353055.2:c.-49+5519… NM_001353055.2:c.-49+5519C>A	N/A	Intron Variant
GSN transcript variant 14	NM_001353056.2:c.-2+4531C… NM_001353056.2:c.-2+4531C>A	N/A	Intron Variant
GSN transcript variant 15	NM_001353057.2:c.-2+5519C… NM_001353057.2:c.-2+5519C>A	N/A	Intron Variant
GSN transcript variant 16	NM_001353058.2:c.-2+5519C… NM_001353058.2:c.-2+5519C>A	N/A	Intron Variant
GSN transcript variant 17	NM_001353059.2:c.-2+4531C… NM_001353059.2:c.-2+4531C>A	N/A	Intron Variant
GSN transcript variant 18	NM_001353060.2:c.-10+5519… NM_001353060.2:c.-10+5519C>A	N/A	Intron Variant
GSN transcript variant 19	NM_001353061.2:c.-10+5519… NM_001353061.2:c.-10+5519C>A	N/A	Intron Variant
GSN transcript variant 20	NM_001353062.1:c.-10+5519… NM_001353062.1:c.-10+5519C>A	N/A	Intron Variant
GSN transcript variant 21	NM_001353063.2:c.-38-1298… NM_001353063.2:c.-38-12984C>A	N/A	Intron Variant
GSN transcript variant 22	NM_001353064.2:c.-48+5519… NM_001353064.2:c.-48+5519C>A	N/A	Intron Variant
GSN transcript variant 23	NM_001353065.2:c.-39+5128… NM_001353065.2:c.-39+5128C>A	N/A	Intron Variant
GSN transcript variant 24	NM_001353066.2:c.-48+5519… NM_001353066.2:c.-48+5519C>A	N/A	Intron Variant
GSN transcript variant 25	NM_001353067.2:c.-47-1297… NM_001353067.2:c.-47-12975C>A	N/A	Intron Variant
GSN transcript variant 26	NM_001353068.2:c.-39+4531… NM_001353068.2:c.-39+4531C>A	N/A	Intron Variant
GSN transcript variant 27	NM_001353069.2:c.-48+896C… NM_001353069.2:c.-48+896C>A	N/A	Intron Variant
GSN transcript variant 28	NM_001353070.2:c.-33+5519… NM_001353070.2:c.-33+5519C>A	N/A	Intron Variant
GSN transcript variant 29	NM_001353071.2:c.-48+320C… NM_001353071.2:c.-48+320C>A	N/A	Intron Variant
GSN transcript variant 30	NM_001353072.2:c.-48+4531… NM_001353072.2:c.-48+4531C>A	N/A	Intron Variant
GSN transcript variant 31	NM_001353073.2:c.-39+4531… NM_001353073.2:c.-39+4531C>A	N/A	Intron Variant
GSN transcript variant 32	NM_001353074.2:c.-48+3689… NM_001353074.2:c.-48+3689C>A	N/A	Intron Variant
GSN transcript variant 34	NM_001353076.2:c.-48+5519… NM_001353076.2:c.-48+5519C>A	N/A	Intron Variant
GSN transcript variant 36	NM_001353078.2:c.-459+551… NM_001353078.2:c.-459+5519C>A	N/A	Intron Variant
GSN transcript variant 2	NM_198252.3:c.-10+5519C>A	N/A	Intron Variant
GSN transcript variant 1	NM_000177.5:c.	N/A	Genic Upstream Transcript Variant
GSN transcript variant 33	NM_001353075.1:c.	N/A	Genic Upstream Transcript Variant
GSN transcript variant 35	NM_001353077.1:c.	N/A	Genic Upstream Transcript Variant
GSN transcript variant X2	XM_011518585.2:c.42+896C>A	N/A	Intron Variant
GSN transcript variant X4	XM_017014645.2:c.15+320C>A	N/A	Intron Variant
GSN transcript variant X1	XM_047423265.1:c.99+4531C… XM_047423265.1:c.99+4531C>A	N/A	Intron Variant
GSN transcript variant X3	XM_047423266.1:c.15+320C>A	N/A	Intron Variant
GSN transcript variant X5	XM_047423267.1:c.-48+5519… XM_047423267.1:c.-48+5519C>A	N/A	Intron Variant
GSN transcript variant X7	XM_047423268.1:c.-39+5519… XM_047423268.1:c.-39+5519C>A	N/A	Intron Variant
GSN transcript variant X9	XM_047423270.1:c.-48+320C… XM_047423270.1:c.-48+320C>A	N/A	Intron Variant
GSN transcript variant X10	XM_047423271.1:c.-39+896C… XM_047423271.1:c.-39+896C>A	N/A	Intron Variant
GSN transcript variant X11	XM_047423272.1:c.-49+5519… XM_047423272.1:c.-49+5519C>A	N/A	Intron Variant
GSN transcript variant X12	XM_047423273.1:c.-10+5128… XM_047423273.1:c.-10+5128C>A	N/A	Intron Variant
GSN transcript variant X6	XM_005251944.2:c.	N/A	Genic Upstream Transcript Variant
GSN transcript variant X13	XM_011518594.2:c.	N/A	Genic Upstream Transcript Variant
GSN transcript variant X8	XM_047423269.1:c.	N/A	Genic Upstream Transcript Variant

Gene: GSN-AS1, GSN antisense RNA 1 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
GSN-AS1 transcript	NR_103560.1: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	C=	A	T
GRCh38.p14 chr 9	NC_000009.12:g.121287081=	NC_000009.12:g.121287081C>A	NC_000009.12:g.121287081C>T
GRCh37.p13 chr 9	NC_000009.11:g.124049359=	NC_000009.11:g.124049359C>A	NC_000009.11:g.124049359C>T
GSN RefSeqGene	NG_012872.2:g.91000=	NG_012872.2:g.91000C>A	NG_012872.2:g.91000C>T
GSN transcript variant 3	NM_001127662.1:c.-9-14882=	NM_001127662.1:c.-9-14882C>A	NM_001127662.1:c.-9-14882C>T
GSN transcript variant 3	NM_001127662.2:c.-9-14882=	NM_001127662.2:c.-9-14882C>A	NM_001127662.2:c.-9-14882C>T
GSN transcript variant 4	NM_001127663.1:c.99+4531=	NM_001127663.1:c.99+4531C>A	NM_001127663.1:c.99+4531C>T
GSN transcript variant 4	NM_001127663.2:c.99+4531=	NM_001127663.2:c.99+4531C>A	NM_001127663.2:c.99+4531C>T
GSN transcript variant 5	NM_001127664.1:c.-10+5128=	NM_001127664.1:c.-10+5128C>A	NM_001127664.1:c.-10+5128C>T
GSN transcript variant 5	NM_001127664.2:c.-10+5128=	NM_001127664.2:c.-10+5128C>A	NM_001127664.2:c.-10+5128C>T
GSN transcript variant 6	NM_001127665.1:c.-10+3689=	NM_001127665.1:c.-10+3689C>A	NM_001127665.1:c.-10+3689C>T
GSN transcript variant 6	NM_001127665.2:c.-10+3689=	NM_001127665.2:c.-10+3689C>A	NM_001127665.2:c.-10+3689C>T
GSN transcript variant 7	NM_001127666.1:c.-48+5519=	NM_001127666.1:c.-48+5519C>A	NM_001127666.1:c.-48+5519C>T
GSN transcript variant 7	NM_001127666.2:c.-48+5519=	NM_001127666.2:c.-48+5519C>A	NM_001127666.2:c.-48+5519C>T
GSN transcript variant 8	NM_001127667.1:c.-39+5519=	NM_001127667.1:c.-39+5519C>A	NM_001127667.1:c.-39+5519C>T
GSN transcript variant 8	NM_001127667.2:c.-39+5519=	NM_001127667.2:c.-39+5519C>A	NM_001127667.2:c.-39+5519C>T
GSN transcript variant 9	NM_001258029.1:c.42+896=	NM_001258029.1:c.42+896C>A	NM_001258029.1:c.42+896C>T
GSN transcript variant 9	NM_001258029.2:c.42+896=	NM_001258029.2:c.42+896C>A	NM_001258029.2:c.42+896C>T
GSN transcript variant 10	NM_001258030.1:c.15+320=	NM_001258030.1:c.15+320C>A	NM_001258030.1:c.15+320C>T
GSN transcript variant 10	NM_001258030.2:c.15+320=	NM_001258030.2:c.15+320C>A	NM_001258030.2:c.15+320C>T
GSN transcript variant 11	NM_001353053.1:c.-10+5519=	NM_001353053.1:c.-10+5519C>A	NM_001353053.1:c.-10+5519C>T
GSN transcript variant 12	NM_001353054.1:c.-10+5519=	NM_001353054.1:c.-10+5519C>A	NM_001353054.1:c.-10+5519C>T
GSN transcript variant 13	NM_001353055.2:c.-49+5519=	NM_001353055.2:c.-49+5519C>A	NM_001353055.2:c.-49+5519C>T
GSN transcript variant 14	NM_001353056.2:c.-2+4531=	NM_001353056.2:c.-2+4531C>A	NM_001353056.2:c.-2+4531C>T
GSN transcript variant 15	NM_001353057.2:c.-2+5519=	NM_001353057.2:c.-2+5519C>A	NM_001353057.2:c.-2+5519C>T
GSN transcript variant 16	NM_001353058.2:c.-2+5519=	NM_001353058.2:c.-2+5519C>A	NM_001353058.2:c.-2+5519C>T
GSN transcript variant 17	NM_001353059.2:c.-2+4531=	NM_001353059.2:c.-2+4531C>A	NM_001353059.2:c.-2+4531C>T
GSN transcript variant 18	NM_001353060.2:c.-10+5519=	NM_001353060.2:c.-10+5519C>A	NM_001353060.2:c.-10+5519C>T
GSN transcript variant 19	NM_001353061.2:c.-10+5519=	NM_001353061.2:c.-10+5519C>A	NM_001353061.2:c.-10+5519C>T
GSN transcript variant 20	NM_001353062.1:c.-10+5519=	NM_001353062.1:c.-10+5519C>A	NM_001353062.1:c.-10+5519C>T
GSN transcript variant 21	NM_001353063.2:c.-38-12984=	NM_001353063.2:c.-38-12984C>A	NM_001353063.2:c.-38-12984C>T
GSN transcript variant 22	NM_001353064.2:c.-48+5519=	NM_001353064.2:c.-48+5519C>A	NM_001353064.2:c.-48+5519C>T
GSN transcript variant 23	NM_001353065.2:c.-39+5128=	NM_001353065.2:c.-39+5128C>A	NM_001353065.2:c.-39+5128C>T
GSN transcript variant 24	NM_001353066.2:c.-48+5519=	NM_001353066.2:c.-48+5519C>A	NM_001353066.2:c.-48+5519C>T
GSN transcript variant 25	NM_001353067.2:c.-47-12975=	NM_001353067.2:c.-47-12975C>A	NM_001353067.2:c.-47-12975C>T
GSN transcript variant 26	NM_001353068.2:c.-39+4531=	NM_001353068.2:c.-39+4531C>A	NM_001353068.2:c.-39+4531C>T
GSN transcript variant 27	NM_001353069.2:c.-48+896=	NM_001353069.2:c.-48+896C>A	NM_001353069.2:c.-48+896C>T
GSN transcript variant 28	NM_001353070.2:c.-33+5519=	NM_001353070.2:c.-33+5519C>A	NM_001353070.2:c.-33+5519C>T
GSN transcript variant 29	NM_001353071.2:c.-48+320=	NM_001353071.2:c.-48+320C>A	NM_001353071.2:c.-48+320C>T
GSN transcript variant 30	NM_001353072.2:c.-48+4531=	NM_001353072.2:c.-48+4531C>A	NM_001353072.2:c.-48+4531C>T
GSN transcript variant 31	NM_001353073.2:c.-39+4531=	NM_001353073.2:c.-39+4531C>A	NM_001353073.2:c.-39+4531C>T
GSN transcript variant 32	NM_001353074.2:c.-48+3689=	NM_001353074.2:c.-48+3689C>A	NM_001353074.2:c.-48+3689C>T
GSN transcript variant 34	NM_001353076.2:c.-48+5519=	NM_001353076.2:c.-48+5519C>A	NM_001353076.2:c.-48+5519C>T
GSN transcript variant 36	NM_001353078.2:c.-459+5519=	NM_001353078.2:c.-459+5519C>A	NM_001353078.2:c.-459+5519C>T
GSN transcript variant 2	NM_198252.2:c.-10+5519=	NM_198252.2:c.-10+5519C>A	NM_198252.2:c.-10+5519C>T
GSN transcript variant 2	NM_198252.3:c.-10+5519=	NM_198252.3:c.-10+5519C>A	NM_198252.3:c.-10+5519C>T
GSN transcript variant X1	XM_005251940.1:c.15+320=	XM_005251940.1:c.15+320C>A	XM_005251940.1:c.15+320C>T
GSN transcript variant X2	XM_005251941.1:c.-39+4531=	XM_005251941.1:c.-39+4531C>A	XM_005251941.1:c.-39+4531C>T
GSN transcript variant X3	XM_005251942.1:c.-39+5128=	XM_005251942.1:c.-39+5128C>A	XM_005251942.1:c.-39+5128C>T
GSN transcript variant X6	XM_005251945.1:c.-49+5519=	XM_005251945.1:c.-49+5519C>A	XM_005251945.1:c.-49+5519C>T
GSN transcript variant X2	XM_011518585.2:c.42+896=	XM_011518585.2:c.42+896C>A	XM_011518585.2:c.42+896C>T
GSN transcript variant X4	XM_017014645.2:c.15+320=	XM_017014645.2:c.15+320C>A	XM_017014645.2:c.15+320C>T
GSN transcript variant X1	XM_047423265.1:c.99+4531=	XM_047423265.1:c.99+4531C>A	XM_047423265.1:c.99+4531C>T
GSN transcript variant X3	XM_047423266.1:c.15+320=	XM_047423266.1:c.15+320C>A	XM_047423266.1:c.15+320C>T
GSN transcript variant X5	XM_047423267.1:c.-48+5519=	XM_047423267.1:c.-48+5519C>A	XM_047423267.1:c.-48+5519C>T
GSN transcript variant X7	XM_047423268.1:c.-39+5519=	XM_047423268.1:c.-39+5519C>A	XM_047423268.1:c.-39+5519C>T
GSN transcript variant X9	XM_047423270.1:c.-48+320=	XM_047423270.1:c.-48+320C>A	XM_047423270.1:c.-48+320C>T
GSN transcript variant X10	XM_047423271.1:c.-39+896=	XM_047423271.1:c.-39+896C>A	XM_047423271.1:c.-39+896C>T
GSN transcript variant X11	XM_047423272.1:c.-49+5519=	XM_047423272.1:c.-49+5519C>A	XM_047423272.1:c.-49+5519C>T
GSN transcript variant X12	XM_047423273.1:c.-10+5128=	XM_047423273.1:c.-10+5128C>A	XM_047423273.1:c.-10+5128C>T

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#.

3 SubSNP, 5 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	GNOMAD	ss2883021971	Nov 08, 2017 (151)
2	TOPMED	ss4835092306	Apr 26, 2021 (155)
3	TOPMED	ss4835092307	Apr 26, 2021 (155)
4	gnomAD - Genomes Submission ignored due to conflicting rows: Row 337173495 (NC_000009.12:121287080:C:A 1/140264) Row 337173496 (NC_000009.12:121287080:C:T 1/140264)	-	Apr 26, 2021 (155)
5	gnomAD - Genomes Submission ignored due to conflicting rows: Row 337173495 (NC_000009.12:121287080:C:A 1/140264) Row 337173496 (NC_000009.12:121287080:C:T 1/140264)	-	Apr 26, 2021 (155)
6	TopMed Submission ignored due to conflicting rows: Row 672469867 (NC_000009.12:121287080:C:A 1/264690) Row 672469868 (NC_000009.12:121287080:C:T 1/264690)	-	Apr 26, 2021 (155)
7	TopMed Submission ignored due to conflicting rows: Row 672469867 (NC_000009.12:121287080:C:A 1/264690) Row 672469868 (NC_000009.12:121287080:C:T 1/264690)	-	Apr 26, 2021 (155)
8	ALFA	NC_000009.12 - 121287081	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
ss2883021971	NC_000009.11:124049358:C:A	NC_000009.12:121287080:C:A	(self)
11011668466, ss4835092306	NC_000009.12:121287080:C:A	NC_000009.12:121287080:C:A	(self)
11011668466, ss4835092307	NC_000009.12:121287080:C:T	NC_000009.12:121287080:C:T	(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 rs1482062110

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

rs1482062110