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dbSNP Short Genetic Variations

Examples: rs268, BRCA1 and more Advanced search

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.

rs139430625

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr16:48210974 (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
G>A
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.001421 (376/264690, TOPMED)
A=0.000330 (83/251146, GnomAD_exome)
A=0.000174 (33/189792, ALFA) (+ 9 more)
A=0.001533 (215/140270, GnomAD)
A=0.000363 (44/121338, ExAC)
A=0.00206 (162/78694, PAGE_STUDY)
A=0.00108 (14/13002, GO-ESP)
A=0.0014 (9/6404, 1000G_30x)
A=0.0012 (6/5008, 1000G)
A=0.005 (1/216, Qatari)
G=0.5 (2/4, SGDP_PRJ)
A=0.5 (2/4, SGDP_PRJ)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
ABCC11 : Missense 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: 20230706150541
Population Group Sample Size Ref Allele Alt Allele
Total Global 206152 G=0.999733 A=0.000267
European Sub 175518 G=0.999943 A=0.000057
African Sub 9788 G=0.9958 A=0.0042
African Others Sub 360 G=0.997 A=0.003
African American Sub 9428 G=0.9958 A=0.0042
Asian Sub 3394 G=1.0000 A=0.0000
East Asian Sub 2712 G=1.0000 A=0.0000
Other Asian Sub 682 G=1.000 A=0.000
Latin American 1 Sub 796 G=0.999 A=0.001
Latin American 2 Sub 968 G=1.000 A=0.000
South Asian Sub 280 G=1.000 A=0.000
Other Sub 15408 G=0.99981 A=0.00019


Help

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").

Download
Study Population Group Sample Size Ref Allele Alt Allele
TopMed Global Study-wide 264690 G=0.998579 A=0.001421
gnomAD - Exomes Global Study-wide 251146 G=0.999670 A=0.000330
gnomAD - Exomes European Sub 135086 G=0.999948 A=0.000052
gnomAD - Exomes Asian Sub 49006 G=1.00000 A=0.00000
gnomAD - Exomes American Sub 34582 G=0.99991 A=0.00009
gnomAD - Exomes African Sub 16256 G=0.99563 A=0.00437
gnomAD - Exomes Ashkenazi Jewish Sub 10080 G=1.00000 A=0.00000
gnomAD - Exomes Other Sub 6136 G=0.9997 A=0.0003
Allele Frequency Aggregator Total Global 189792 G=0.999826 A=0.000174
Allele Frequency Aggregator European Sub 165424 G=0.999952 A=0.000048
Allele Frequency Aggregator Other Sub 13976 G=0.99986 A=0.00014
Allele Frequency Aggregator African Sub 4954 G=0.9956 A=0.0044
Allele Frequency Aggregator Asian Sub 3394 G=1.0000 A=0.0000
Allele Frequency Aggregator Latin American 2 Sub 968 G=1.000 A=0.000
Allele Frequency Aggregator Latin American 1 Sub 796 G=0.999 A=0.001
Allele Frequency Aggregator South Asian Sub 280 G=1.000 A=0.000
gnomAD - Genomes Global Study-wide 140270 G=0.998467 A=0.001533
gnomAD - Genomes European Sub 75950 G=0.99997 A=0.00003
gnomAD - Genomes African Sub 42058 G=0.99501 A=0.00499
gnomAD - Genomes American Sub 13654 G=0.99978 A=0.00022
gnomAD - Genomes Ashkenazi Jewish Sub 3324 G=1.0000 A=0.0000
gnomAD - Genomes East Asian Sub 3132 G=1.0000 A=0.0000
gnomAD - Genomes Other Sub 2152 G=1.0000 A=0.0000
ExAC Global Study-wide 121338 G=0.999637 A=0.000363
ExAC Europe Sub 73298 G=0.99996 A=0.00004
ExAC Asian Sub 25160 G=1.00000 A=0.00000
ExAC American Sub 11572 G=0.99991 A=0.00009
ExAC African Sub 10400 G=0.99615 A=0.00385
ExAC Other Sub 908 G=1.000 A=0.000
The PAGE Study Global Study-wide 78694 G=0.99794 A=0.00206
The PAGE Study AfricanAmerican Sub 32514 G=0.99597 A=0.00403
The PAGE Study Mexican Sub 10810 G=0.99972 A=0.00028
The PAGE Study Asian Sub 8318 G=1.0000 A=0.0000
The PAGE Study PuertoRican Sub 7918 G=0.9989 A=0.0011
The PAGE Study NativeHawaiian Sub 4534 G=0.9998 A=0.0002
The PAGE Study Cuban Sub 4228 G=0.9979 A=0.0021
The PAGE Study Dominican Sub 3826 G=0.9987 A=0.0013
The PAGE Study CentralAmerican Sub 2448 G=0.9996 A=0.0004
The PAGE Study SouthAmerican Sub 1982 G=0.9985 A=0.0015
The PAGE Study NativeAmerican Sub 1260 G=1.0000 A=0.0000
The PAGE Study SouthAsian Sub 856 G=1.000 A=0.000
GO Exome Sequencing Project Global Study-wide 13002 G=0.99892 A=0.00108
GO Exome Sequencing Project European American Sub 8600 G=1.0000 A=0.0000
GO Exome Sequencing Project African American Sub 4402 G=0.9968 A=0.0032
1000Genomes_30x Global Study-wide 6404 G=0.9986 A=0.0014
1000Genomes_30x African Sub 1786 G=0.9950 A=0.0050
1000Genomes_30x Europe Sub 1266 G=1.0000 A=0.0000
1000Genomes_30x South Asian Sub 1202 G=1.0000 A=0.0000
1000Genomes_30x East Asian Sub 1170 G=1.0000 A=0.0000
1000Genomes_30x American Sub 980 G=1.000 A=0.000
1000Genomes Global Study-wide 5008 G=0.9988 A=0.0012
1000Genomes African Sub 1322 G=0.9955 A=0.0045
1000Genomes East Asian Sub 1008 G=1.0000 A=0.0000
1000Genomes Europe Sub 1006 G=1.0000 A=0.0000
1000Genomes South Asian Sub 978 G=1.000 A=0.000
1000Genomes American Sub 694 G=1.000 A=0.000
Qatari Global Study-wide 216 G=0.995 A=0.005
SGDP_PRJ Global Study-wide 4 G=0.5 A=0.5
Help

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 16 NC_000016.10:g.48210974G>A
GRCh37.p13 chr 16 NC_000016.9:g.48244885G>A
ABCC11 RefSeqGene NG_011522.1:g.29204C>T
Gene: ABCC11, ATP binding cassette subfamily C member 11 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
ABCC11 transcript variant 4 NM_001370496.1:c.1582C>T H [CAC] > Y [TAC] Coding Sequence Variant
ATP-binding cassette sub-family C member 11 isoform c NP_001357425.1:p.His528Tyr H (His) > Y (Tyr) Missense Variant
ABCC11 transcript variant 2 NM_033151.4:c.1582C>T H [CAC] > Y [TAC] Coding Sequence Variant
ATP-binding cassette sub-family C member 11 isoform a NP_149163.2:p.His528Tyr H (His) > Y (Tyr) Missense Variant
ABCC11 transcript variant 3 NM_145186.3:c.1582C>T H [CAC] > Y [TAC] Coding Sequence Variant
ATP-binding cassette sub-family C member 11 isoform b NP_660187.1:p.His528Tyr H (His) > Y (Tyr) Missense Variant
ABCC11 transcript variant 1 NM_032583.4:c.1582C>T H [CAC] > Y [TAC] Coding Sequence Variant
ATP-binding cassette sub-family C member 11 isoform a NP_115972.2:p.His528Tyr H (His) > Y (Tyr) Missense Variant
ABCC11 transcript variant 5 NM_001370497.1:c.1582C>T H [CAC] > Y [TAC] Coding Sequence Variant
ATP-binding cassette sub-family C member 11 isoform a NP_001357426.1:p.His528Tyr H (His) > Y (Tyr) Missense Variant
ABCC11 transcript variant X10 XM_011523398.4:c. N/A Genic Upstream Transcript Variant
ABCC11 transcript variant X1 XM_017023799.3:c.1582C>T H [CAC] > Y [TAC] Coding Sequence Variant
ATP-binding cassette sub-family C member 11 isoform X1 XP_016879288.1:p.His528Tyr H (His) > Y (Tyr) Missense Variant
ABCC11 transcript variant X2 XM_017023798.3:c.1582C>T H [CAC] > Y [TAC] Coding Sequence Variant
ATP-binding cassette sub-family C member 11 isoform X1 XP_016879287.1:p.His528Tyr H (His) > Y (Tyr) Missense Variant
ABCC11 transcript variant X3 XM_017023797.3:c.1582C>T H [CAC] > Y [TAC] Coding Sequence Variant
ATP-binding cassette sub-family C member 11 isoform X1 XP_016879286.1:p.His528Tyr H (His) > Y (Tyr) Missense Variant
ABCC11 transcript variant X4 XM_017023800.3:c.1582C>T H [CAC] > Y [TAC] Coding Sequence Variant
ATP-binding cassette sub-family C member 11 isoform X1 XP_016879289.1:p.His528Tyr H (His) > Y (Tyr) Missense Variant
ABCC11 transcript variant X6 XM_017023801.3:c.1474C>T H [CAC] > Y [TAC] Coding Sequence Variant
ATP-binding cassette sub-family C member 11 isoform X2 XP_016879290.1:p.His492Tyr H (His) > Y (Tyr) Missense Variant
ABCC11 transcript variant X7 XM_017023802.3:c.625C>T H [CAC] > Y [TAC] Coding Sequence Variant
ATP-binding cassette sub-family C member 11 isoform X3 XP_016879291.1:p.His209Tyr H (His) > Y (Tyr) Missense Variant
ABCC11 transcript variant X8 XM_024450475.2:c.625C>T H [CAC] > Y [TAC] Coding Sequence Variant
ATP-binding cassette sub-family C member 11 isoform X3 XP_024306243.1:p.His209Tyr H (His) > Y (Tyr) Missense Variant
ABCC11 transcript variant X9 XM_047434818.1:c.1582C>T H [CAC] > Y [TAC] Coding Sequence Variant
ATP-binding cassette sub-family C member 11 isoform X4 XP_047290774.1:p.His528Tyr H (His) > Y (Tyr) Missense Variant
ABCC11 transcript variant X5 XR_007064925.1:n.1980C>T N/A Non Coding Transcript Variant
Help

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
Help

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 G= A
GRCh38.p14 chr 16 NC_000016.10:g.48210974= NC_000016.10:g.48210974G>A
GRCh37.p13 chr 16 NC_000016.9:g.48244885= NC_000016.9:g.48244885G>A
ABCC11 RefSeqGene NG_011522.1:g.29204= NG_011522.1:g.29204C>T
ABCC11 transcript variant 2 NM_033151.3:c.1582= NM_033151.3:c.1582C>T
ABCC11 transcript variant 2 NM_033151.4:c.1582= NM_033151.4:c.1582C>T
ABCC11 transcript variant 1 NM_032583.3:c.1582= NM_032583.3:c.1582C>T
ABCC11 transcript variant 1 NM_032583.4:c.1582= NM_032583.4:c.1582C>T
ABCC11 transcript variant 3 NM_145186.2:c.1582= NM_145186.2:c.1582C>T
ABCC11 transcript variant 3 NM_145186.3:c.1582= NM_145186.3:c.1582C>T
ABCC11 transcript variant X1 XM_017023799.3:c.1582= XM_017023799.3:c.1582C>T
ABCC11 transcript variant X5 XM_017023799.2:c.1582= XM_017023799.2:c.1582C>T
ABCC11 transcript variant X5 XM_017023799.1:c.1582= XM_017023799.1:c.1582C>T
ABCC11 transcript variant X4 XM_017023800.3:c.1582= XM_017023800.3:c.1582C>T
ABCC11 transcript variant X6 XM_017023800.2:c.1582= XM_017023800.2:c.1582C>T
ABCC11 transcript variant X6 XM_017023800.1:c.1582= XM_017023800.1:c.1582C>T
ABCC11 transcript variant X6 XM_017023801.3:c.1474= XM_017023801.3:c.1474C>T
ABCC11 transcript variant X8 XM_017023801.2:c.1474= XM_017023801.2:c.1474C>T
ABCC11 transcript variant X8 XM_017023801.1:c.1474= XM_017023801.1:c.1474C>T
ABCC11 transcript variant X3 XM_017023797.3:c.1582= XM_017023797.3:c.1582C>T
ABCC11 transcript variant X3 XM_017023797.2:c.1582= XM_017023797.2:c.1582C>T
ABCC11 transcript variant X3 XM_017023797.1:c.1582= XM_017023797.1:c.1582C>T
ABCC11 transcript variant X2 XM_017023798.3:c.1582= XM_017023798.3:c.1582C>T
ABCC11 transcript variant X4 XM_017023798.2:c.1582= XM_017023798.2:c.1582C>T
ABCC11 transcript variant X4 XM_017023798.1:c.1582= XM_017023798.1:c.1582C>T
ABCC11 transcript variant X7 XM_017023802.3:c.625= XM_017023802.3:c.625C>T
ABCC11 transcript variant X10 XM_017023802.2:c.625= XM_017023802.2:c.625C>T
ABCC11 transcript variant X10 XM_017023802.1:c.625= XM_017023802.1:c.625C>T
ABCC11 transcript variant X8 XM_024450475.2:c.625= XM_024450475.2:c.625C>T
ABCC11 transcript variant X11 XM_024450475.1:c.625= XM_024450475.1:c.625C>T
ABCC11 transcript variant 4 NM_001370496.1:c.1582= NM_001370496.1:c.1582C>T
ABCC11 transcript variant 5 NM_001370497.1:c.1582= NM_001370497.1:c.1582C>T
ABCC11 transcript variant X5 XR_007064925.1:n.1980= XR_007064925.1:n.1980C>T
ABCC11 transcript variant X9 XM_047434818.1:c.1582= XM_047434818.1:c.1582C>T
ATP-binding cassette sub-family C member 11 isoform a NP_149163.2:p.His528= NP_149163.2:p.His528Tyr
ATP-binding cassette sub-family C member 11 isoform a NP_115972.2:p.His528= NP_115972.2:p.His528Tyr
ATP-binding cassette sub-family C member 11 isoform b NP_660187.1:p.His528= NP_660187.1:p.His528Tyr
ATP-binding cassette sub-family C member 11 isoform X1 XP_016879288.1:p.His528= XP_016879288.1:p.His528Tyr
ATP-binding cassette sub-family C member 11 isoform X1 XP_016879289.1:p.His528= XP_016879289.1:p.His528Tyr
ATP-binding cassette sub-family C member 11 isoform X2 XP_016879290.1:p.His492= XP_016879290.1:p.His492Tyr
ATP-binding cassette sub-family C member 11 isoform X1 XP_016879286.1:p.His528= XP_016879286.1:p.His528Tyr
ATP-binding cassette sub-family C member 11 isoform X1 XP_016879287.1:p.His528= XP_016879287.1:p.His528Tyr
ATP-binding cassette sub-family C member 11 isoform X3 XP_016879291.1:p.His209= XP_016879291.1:p.His209Tyr
ATP-binding cassette sub-family C member 11 isoform X3 XP_024306243.1:p.His209= XP_024306243.1:p.His209Tyr
ATP-binding cassette sub-family C member 11 isoform c NP_001357425.1:p.His528= NP_001357425.1:p.His528Tyr
ATP-binding cassette sub-family C member 11 isoform a NP_001357426.1:p.His528= NP_001357426.1:p.His528Tyr
ATP-binding cassette sub-family C member 11 isoform X4 XP_047290774.1:p.His528= XP_047290774.1:p.His528Tyr
Help

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#.

42 SubSNP, 11 Frequency submissions
No Submitter Submission ID Date (Build)
1 NHLBI-ESP ss342427873 May 09, 2011 (134)
2 1000GENOMES ss489079159 May 04, 2012 (137)
3 EXOME_CHIP ss491507960 May 04, 2012 (137)
4 ILLUMINA ss780718355 Sep 08, 2015 (146)
5 ILLUMINA ss783393854 Sep 08, 2015 (146)
6 1000GENOMES ss1356131421 Aug 21, 2014 (142)
7 EVA_EXAC ss1692288716 Apr 01, 2015 (144)
8 ILLUMINA ss1752192410 Sep 08, 2015 (146)
9 ILLUMINA ss1917907209 Feb 12, 2016 (147)
10 WEILL_CORNELL_DGM ss1935895500 Feb 12, 2016 (147)
11 ILLUMINA ss1946414212 Feb 12, 2016 (147)
12 ILLUMINA ss1959676225 Feb 12, 2016 (147)
13 HUMAN_LONGEVITY ss2211917620 Dec 20, 2016 (150)
14 GNOMAD ss2741964735 Nov 08, 2017 (151)
15 GNOMAD ss2749536701 Nov 08, 2017 (151)
16 GNOMAD ss2942699600 Nov 08, 2017 (151)
17 AFFY ss2985067795 Nov 08, 2017 (151)
18 ILLUMINA ss3021703209 Nov 08, 2017 (151)
19 ILLUMINA ss3627516016 Oct 12, 2018 (152)
20 ILLUMINA ss3634640659 Oct 12, 2018 (152)
21 ILLUMINA ss3640347978 Oct 12, 2018 (152)
22 ILLUMINA ss3644667275 Oct 12, 2018 (152)
23 ILLUMINA ss3652111180 Oct 12, 2018 (152)
24 ILLUMINA ss3653839515 Oct 12, 2018 (152)
25 ILLUMINA ss3725559261 Jul 13, 2019 (153)
26 ILLUMINA ss3744431879 Jul 13, 2019 (153)
27 ILLUMINA ss3744941083 Jul 13, 2019 (153)
28 PAGE_CC ss3771877364 Jul 13, 2019 (153)
29 ILLUMINA ss3772439384 Jul 13, 2019 (153)
30 KHV_HUMAN_GENOMES ss3819192424 Jul 13, 2019 (153)
31 EVA ss3825013040 Apr 27, 2020 (154)
32 SGDP_PRJ ss3884381426 Apr 27, 2020 (154)
33 EVA ss3986686109 Apr 26, 2021 (155)
34 TOPMED ss5014396813 Apr 26, 2021 (155)
35 1000G_HIGH_COVERAGE ss5300863643 Oct 17, 2022 (156)
36 EVA ss5423530737 Oct 17, 2022 (156)
37 HUGCELL_USP ss5494220783 Oct 17, 2022 (156)
38 1000G_HIGH_COVERAGE ss5603461331 Oct 17, 2022 (156)
39 SANFORD_IMAGENETICS ss5658850347 Oct 17, 2022 (156)
40 EVA ss5847769987 Oct 17, 2022 (156)
41 EVA ss5898983025 Oct 17, 2022 (156)
42 EVA ss5950235923 Oct 17, 2022 (156)
43 1000Genomes NC_000016.9 - 48244885 Oct 12, 2018 (152)
44 1000Genomes_30x NC_000016.10 - 48210974 Oct 17, 2022 (156)
45 ExAC NC_000016.9 - 48244885 Oct 12, 2018 (152)
46 gnomAD - Genomes NC_000016.10 - 48210974 Apr 26, 2021 (155)
47 gnomAD - Exomes NC_000016.9 - 48244885 Jul 13, 2019 (153)
48 GO Exome Sequencing Project NC_000016.9 - 48244885 Oct 12, 2018 (152)
49 The PAGE Study NC_000016.10 - 48210974 Jul 13, 2019 (153)
50 Qatari NC_000016.9 - 48244885 Apr 27, 2020 (154)
51 SGDP_PRJ NC_000016.9 - 48244885 Apr 27, 2020 (154)
52 TopMed NC_000016.10 - 48210974 Apr 26, 2021 (155)
53 ALFA NC_000016.10 - 48210974 Apr 26, 2021 (155)
Help

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
69290166, 2695441, 11243574, 1470217, 17937422, 36398406, ss342427873, ss489079159, ss491507960, ss780718355, ss783393854, ss1356131421, ss1692288716, ss1752192410, ss1917907209, ss1935895500, ss1946414212, ss1959676225, ss2741964735, ss2749536701, ss2942699600, ss2985067795, ss3021703209, ss3627516016, ss3634640659, ss3640347978, ss3644667275, ss3652111180, ss3653839515, ss3744431879, ss3744941083, ss3772439384, ss3825013040, ss3884381426, ss3986686109, ss5423530737, ss5658850347, ss5847769987, ss5950235923 NC_000016.9:48244884:G:A NC_000016.10:48210973:G:A (self)
90987266, 488773456, 1098833, 229942474, 3122887493, ss2211917620, ss3725559261, ss3771877364, ss3819192424, ss5014396813, ss5300863643, ss5494220783, ss5603461331, ss5898983025 NC_000016.10:48210973:G:A NC_000016.10:48210973:G:A (self)
Help

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

No publications for rs139430625

Help

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.

Software version is: 2.0.1.post761+d5e8e07