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dbSNP Short Genetic Variations

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.

rs9306235

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr22:19967634 (GRCh38.p13) 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 / G>T
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.049726 (13162/264690, TOPMED)
A=0.071506 (10689/149484, ALFA)
A=0.049638 (6959/140196, GnomAD) (+ 12 more)
A=0.00006 (1/16760, 8.3KJPN)
A=0.0282 (141/5008, 1000G)
A=0.0507 (227/4480, Estonian)
A=0.0394 (57/1446, HapMap)
A=0.080 (80/998, GoNL)
A=0.053 (32/600, NorthernSweden)
A=0.046 (10/216, Qatari)
A=0.10 (4/40, GENOME_DK)
G=0.5 (4/8, SGDP_PRJ)
A=0.5 (4/8, SGDP_PRJ)
G=0.5 (2/4, Siberian)
A=0.5 (2/4, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
ARVCF : Intron Variant
COMT : Intron Variant
Publications
1 citation
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: 20201027095038
Population Group Sample Size Ref Allele Alt Allele
Total Global 149484 G=0.928494 A=0.071506
European Sub 128668 G=0.923299 A=0.076701
African Sub 6678 G=0.9868 A=0.0132
African Others Sub 242 G=0.996 A=0.004
African American Sub 6436 G=0.9865 A=0.0135
Asian Sub 630 G=1.000 A=0.000
East Asian Sub 498 G=1.000 A=0.000
Other Asian Sub 132 G=1.000 A=0.000
Latin American 1 Sub 752 G=0.916 A=0.084
Latin American 2 Sub 6332 G=0.9616 A=0.0384
South Asian Sub 184 G=0.973 A=0.027
Other Sub 6240 G=0.9325 A=0.0675


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=0.950274 A=0.049726
Allele Frequency Aggregator Total Global 149484 G=0.928494 A=0.071506
Allele Frequency Aggregator European Sub 128668 G=0.923299 A=0.076701
Allele Frequency Aggregator African Sub 6678 G=0.9868 A=0.0132
Allele Frequency Aggregator Latin American 2 Sub 6332 G=0.9616 A=0.0384
Allele Frequency Aggregator Other Sub 6240 G=0.9325 A=0.0675
Allele Frequency Aggregator Latin American 1 Sub 752 G=0.916 A=0.084
Allele Frequency Aggregator Asian Sub 630 G=1.000 A=0.000
Allele Frequency Aggregator South Asian Sub 184 G=0.973 A=0.027
gnomAD - Genomes Global Study-wide 140196 G=0.950362 A=0.049638
gnomAD - Genomes European Sub 75930 G=0.93181 A=0.06819
gnomAD - Genomes African Sub 42012 G=0.98631 A=0.01369
gnomAD - Genomes American Sub 13648 G=0.93860 A=0.06140
gnomAD - Genomes Ashkenazi Jewish Sub 3320 G=0.9241 A=0.0759
gnomAD - Genomes East Asian Sub 3134 G=1.0000 A=0.0000
gnomAD - Genomes Other Sub 2152 G=0.9461 A=0.0539
8.3KJPN JAPANESE Study-wide 16760 G=0.99994 A=0.00006
1000Genomes Global Study-wide 5008 G=0.9718 A=0.0282
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=0.9215 A=0.0785
1000Genomes South Asian Sub 978 G=0.992 A=0.008
1000Genomes American Sub 694 G=0.931 A=0.069
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.9493 A=0.0507
HapMap Global Study-wide 1446 G=0.9606 A=0.0394
HapMap American Sub 600 G=0.958 A=0.042
HapMap African Sub 582 G=0.990 A=0.010
HapMap Europe Sub 176 G=0.852 A=0.148
HapMap Asian Sub 88 G=1.00 A=0.00
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.920 A=0.080
Northern Sweden ACPOP Study-wide 600 G=0.947 A=0.053
Qatari Global Study-wide 216 G=0.954 A=0.046
The Danish reference pan genome Danish Study-wide 40 G=0.90 A=0.10
SGDP_PRJ Global Study-wide 8 G=0.5 A=0.5
Siberian 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.p13 chr 22 NC_000022.11:g.19967634G>A
GRCh38.p13 chr 22 NC_000022.11:g.19967634G>T
GRCh37.p13 chr 22 NC_000022.10:g.19955157G>A
GRCh37.p13 chr 22 NC_000022.10:g.19955157G>T
COMT RefSeqGene (LRG_1010) NG_011526.1:g.30895G>A
COMT RefSeqGene (LRG_1010) NG_011526.1:g.30895G>T
Gene: COMT, catechol-O-methyltransferase (plus strand)
Molecule type Change Amino acid[Codon] SO Term
COMT transcript variant 1 NM_000754.4:c.616-902G>A N/A Intron Variant
COMT transcript variant 2 NM_001135161.2:c.616-902G…

NM_001135161.2:c.616-902G>A

N/A Intron Variant
COMT transcript variant 3 NM_001135162.2:c.616-902G…

NM_001135162.2:c.616-902G>A

N/A Intron Variant
COMT transcript variant 5 NM_001362828.2:c.616-902G…

NM_001362828.2:c.616-902G>A

N/A Intron Variant
COMT transcript variant 4 NM_007310.3:c.466-902G>A N/A Intron Variant
Gene: ARVCF, ARVCF delta catenin family member (minus strand)
Molecule type Change Amino acid[Codon] SO Term
ARVCF transcript variant 1 NM_001670.3:c. N/A Genic Downstream Transcript Variant
ARVCF transcript variant X2 XM_005261242.3:c.2764-425…

XM_005261242.3:c.2764-425C>T

N/A Intron Variant
ARVCF transcript variant X1 XM_006724243.3:c.2782-425…

XM_006724243.3:c.2782-425C>T

N/A Intron Variant
ARVCF transcript variant X8 XM_006724246.4:c.2536-425…

XM_006724246.4:c.2536-425C>T

N/A Intron Variant
ARVCF transcript variant X3 XM_011530179.3:c.2749-425…

XM_011530179.3:c.2749-425C>T

N/A Intron Variant
ARVCF transcript variant X17 XM_011530182.3:c.1348-425…

XM_011530182.3:c.1348-425C>T

N/A Intron Variant
ARVCF transcript variant X9 XM_024452249.1:c.2536-425…

XM_024452249.1:c.2536-425C>T

N/A Intron Variant
ARVCF transcript variant X5 XM_005261243.4:c. N/A Genic Downstream Transcript Variant
ARVCF transcript variant X7 XM_005261244.4:c. N/A Genic Downstream Transcript Variant
ARVCF transcript variant X6 XM_006724245.3:c. N/A Genic Downstream Transcript Variant
ARVCF transcript variant X10 XM_006724247.4:c. N/A Genic Downstream Transcript Variant
ARVCF transcript variant X11 XM_006724248.4:c. N/A Genic Downstream Transcript Variant
ARVCF transcript variant X14 XM_006724249.3:c. N/A Genic Downstream Transcript Variant
ARVCF transcript variant X15 XM_006724250.3:c. N/A Genic Downstream Transcript Variant
ARVCF transcript variant X4 XM_011530180.1:c. N/A Genic Downstream Transcript Variant
ARVCF transcript variant X16 XM_011530181.1:c. N/A Genic Downstream Transcript Variant
ARVCF transcript variant X18 XM_011530183.3:c. N/A Genic Downstream Transcript Variant
ARVCF transcript variant X12 XR_937863.2:n. N/A Genic Downstream Transcript Variant
ARVCF transcript variant X13 XR_937864.1:n. N/A Genic Downstream 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 T
GRCh38.p13 chr 22 NC_000022.11:g.19967634= NC_000022.11:g.19967634G>A NC_000022.11:g.19967634G>T
GRCh37.p13 chr 22 NC_000022.10:g.19955157= NC_000022.10:g.19955157G>A NC_000022.10:g.19955157G>T
COMT RefSeqGene (LRG_1010) NG_011526.1:g.30895= NG_011526.1:g.30895G>A NG_011526.1:g.30895G>T
COMT transcript variant 1 NM_000754.3:c.616-902= NM_000754.3:c.616-902G>A NM_000754.3:c.616-902G>T
COMT transcript variant 1 NM_000754.4:c.616-902= NM_000754.4:c.616-902G>A NM_000754.4:c.616-902G>T
COMT transcript variant 2 NM_001135161.1:c.616-902= NM_001135161.1:c.616-902G>A NM_001135161.1:c.616-902G>T
COMT transcript variant 2 NM_001135161.2:c.616-902= NM_001135161.2:c.616-902G>A NM_001135161.2:c.616-902G>T
COMT transcript variant 3 NM_001135162.1:c.616-902= NM_001135162.1:c.616-902G>A NM_001135162.1:c.616-902G>T
COMT transcript variant 3 NM_001135162.2:c.616-902= NM_001135162.2:c.616-902G>A NM_001135162.2:c.616-902G>T
COMT transcript variant 5 NM_001362828.2:c.616-902= NM_001362828.2:c.616-902G>A NM_001362828.2:c.616-902G>T
COMT transcript variant 4 NM_007310.2:c.466-902= NM_007310.2:c.466-902G>A NM_007310.2:c.466-902G>T
COMT transcript variant 4 NM_007310.3:c.466-902= NM_007310.3:c.466-902G>A NM_007310.3:c.466-902G>T
COMT transcript variant X1 XM_005261229.1:c.616-902= XM_005261229.1:c.616-902G>A XM_005261229.1:c.616-902G>T
ARVCF transcript variant X2 XM_005261242.1:c.2764-425= XM_005261242.1:c.2764-425C>T XM_005261242.1:c.2764-425C>A
ARVCF transcript variant X2 XM_005261242.3:c.2764-425= XM_005261242.3:c.2764-425C>T XM_005261242.3:c.2764-425C>A
ARVCF transcript variant X1 XM_006724243.3:c.2782-425= XM_006724243.3:c.2782-425C>T XM_006724243.3:c.2782-425C>A
ARVCF transcript variant X8 XM_006724246.4:c.2536-425= XM_006724246.4:c.2536-425C>T XM_006724246.4:c.2536-425C>A
ARVCF transcript variant X3 XM_011530179.3:c.2749-425= XM_011530179.3:c.2749-425C>T XM_011530179.3:c.2749-425C>A
ARVCF transcript variant X17 XM_011530182.3:c.1348-425= XM_011530182.3:c.1348-425C>T XM_011530182.3:c.1348-425C>A
ARVCF transcript variant X9 XM_024452249.1:c.2536-425= XM_024452249.1:c.2536-425C>T XM_024452249.1:c.2536-425C>A
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#.

69 SubSNP, 17 Frequency submissions
No Submitter Submission ID Date (Build)
1 EGP_SNPS ss12673788 Dec 05, 2003 (119)
2 SC_SNP ss13346918 Dec 05, 2003 (119)
3 CSHL-HAPMAP ss16926321 Feb 27, 2004 (120)
4 EGP_SNPS ss66862098 Dec 03, 2006 (127)
5 ILLUMINA ss75253638 Dec 06, 2007 (129)
6 KRIBB_YJKIM ss119588336 Dec 01, 2009 (131)
7 ILLUMINA ss160974848 Dec 01, 2009 (131)
8 ILLUMINA ss174802312 Jul 04, 2010 (132)
9 1000GENOMES ss238022318 Jul 15, 2010 (132)
10 PJP ss292736330 May 09, 2011 (134)
11 ILLUMINA ss481860336 May 04, 2012 (137)
12 ILLUMINA ss481893104 May 04, 2012 (137)
13 ILLUMINA ss482853184 Sep 08, 2015 (146)
14 ILLUMINA ss485724506 May 04, 2012 (137)
15 ILLUMINA ss537584024 Sep 08, 2015 (146)
16 ILLUMINA ss778634790 Sep 08, 2015 (146)
17 ILLUMINA ss783307921 Sep 08, 2015 (146)
18 ILLUMINA ss784260093 Sep 08, 2015 (146)
19 ILLUMINA ss832569336 Sep 08, 2015 (146)
20 ILLUMINA ss834092448 Sep 08, 2015 (146)
21 EVA-GONL ss995222837 Aug 21, 2014 (142)
22 1000GENOMES ss1366683250 Aug 21, 2014 (142)
23 DDI ss1429219798 Apr 01, 2015 (144)
24 EVA_GENOME_DK ss1579704284 Apr 01, 2015 (144)
25 EVA_UK10K_ALSPAC ss1639754012 Apr 01, 2015 (144)
26 EVA_UK10K_ALSPAC ss1639754013 Apr 01, 2015 (144)
27 EVA_UK10K_TWINSUK ss1682748045 Apr 01, 2015 (144)
28 EVA_UK10K_TWINSUK ss1682748046 Apr 01, 2015 (144)
29 EVA_DECODE ss1699291938 Apr 01, 2015 (144)
30 EVA_SVP ss1713731254 Apr 01, 2015 (144)
31 ILLUMINA ss1752413986 Sep 08, 2015 (146)
32 WEILL_CORNELL_DGM ss1938784432 Feb 12, 2016 (147)
33 JJLAB ss2030165236 Sep 14, 2016 (149)
34 USC_VALOUEV ss2158775191 Dec 20, 2016 (150)
35 HUMAN_LONGEVITY ss2246457313 Dec 20, 2016 (150)
36 TOPMED ss2413284211 Dec 20, 2016 (150)
37 ILLUMINA ss2633862792 Nov 08, 2017 (151)
38 GNOMAD ss2972986684 Nov 08, 2017 (151)
39 AFFY ss2985850733 Nov 08, 2017 (151)
40 SWEGEN ss3019086418 Nov 08, 2017 (151)
41 BIOINF_KMB_FNS_UNIBA ss3028920334 Nov 08, 2017 (151)
42 CSHL ss3352776510 Nov 08, 2017 (151)
43 TOPMED ss3374061991 Nov 08, 2017 (151)
44 ILLUMINA ss3628506032 Oct 12, 2018 (152)
45 ILLUMINA ss3631815179 Oct 12, 2018 (152)
46 ILLUMINA ss3633268870 Oct 12, 2018 (152)
47 ILLUMINA ss3633984261 Oct 12, 2018 (152)
48 ILLUMINA ss3634860959 Oct 12, 2018 (152)
49 ILLUMINA ss3635668897 Oct 12, 2018 (152)
50 ILLUMINA ss3636556593 Oct 12, 2018 (152)
51 ILLUMINA ss3637421091 Oct 12, 2018 (152)
52 ILLUMINA ss3638374453 Oct 12, 2018 (152)
53 ILLUMINA ss3640568260 Oct 12, 2018 (152)
54 ILLUMINA ss3643334861 Oct 12, 2018 (152)
55 EGCUT_WGS ss3685618938 Jul 13, 2019 (153)
56 EVA_DECODE ss3707955024 Jul 13, 2019 (153)
57 ACPOP ss3743823310 Jul 13, 2019 (153)
58 ILLUMINA ss3745160790 Jul 13, 2019 (153)
59 EVA ss3759230967 Jul 13, 2019 (153)
60 ILLUMINA ss3772656773 Jul 13, 2019 (153)
61 KHV_HUMAN_GENOMES ss3822398855 Jul 13, 2019 (153)
62 EVA ss3825965524 Apr 27, 2020 (154)
63 EVA ss3835927819 Apr 27, 2020 (154)
64 EVA ss3841592413 Apr 27, 2020 (154)
65 EVA ss3847107073 Apr 27, 2020 (154)
66 SGDP_PRJ ss3890256870 Apr 27, 2020 (154)
67 EVA ss4017873662 Apr 26, 2021 (155)
68 TOPMED ss5105109229 Apr 26, 2021 (155)
69 TOMMO_GENOMICS ss5232040714 Apr 26, 2021 (155)
70 1000Genomes NC_000022.10 - 19955157 Oct 12, 2018 (152)
71 The Avon Longitudinal Study of Parents and Children

Submission ignored due to conflicting rows:
Row 44382086 (NC_000022.10:19955156:G:G 3574/3854, NC_000022.10:19955156:G:A 280/3854)
Row 44382087 (NC_000022.10:19955156:G:G 3854/3854, NC_000022.10:19955156:G:T 0/3854)

- Oct 12, 2018 (152)
72 The Avon Longitudinal Study of Parents and Children

Submission ignored due to conflicting rows:
Row 44382086 (NC_000022.10:19955156:G:G 3574/3854, NC_000022.10:19955156:G:A 280/3854)
Row 44382087 (NC_000022.10:19955156:G:G 3854/3854, NC_000022.10:19955156:G:T 0/3854)

- Oct 12, 2018 (152)
73 Genetic variation in the Estonian population NC_000022.10 - 19955157 Oct 12, 2018 (152)
74 The Danish reference pan genome NC_000022.10 - 19955157 Apr 27, 2020 (154)
75 gnomAD - Genomes NC_000022.11 - 19967634 Apr 26, 2021 (155)
76 Genome of the Netherlands Release 5 NC_000022.10 - 19955157 Apr 27, 2020 (154)
77 HapMap NC_000022.11 - 19967634 Apr 27, 2020 (154)
78 Northern Sweden NC_000022.10 - 19955157 Jul 13, 2019 (153)
79 Qatari NC_000022.10 - 19955157 Apr 27, 2020 (154)
80 SGDP_PRJ NC_000022.10 - 19955157 Apr 27, 2020 (154)
81 Siberian NC_000022.10 - 19955157 Apr 27, 2020 (154)
82 8.3KJPN NC_000022.10 - 19955157 Apr 26, 2021 (155)
83 TopMed NC_000022.11 - 19967634 Apr 26, 2021 (155)
84 UK 10K study - Twins

Submission ignored due to conflicting rows:
Row 44382086 (NC_000022.10:19955156:G:G 3415/3708, NC_000022.10:19955156:G:A 293/3708)
Row 44382087 (NC_000022.10:19955156:G:G 3707/3708, NC_000022.10:19955156:G:T 1/3708)

- Oct 12, 2018 (152)
85 UK 10K study - Twins

Submission ignored due to conflicting rows:
Row 44382086 (NC_000022.10:19955156:G:G 3415/3708, NC_000022.10:19955156:G:A 293/3708)
Row 44382087 (NC_000022.10:19955156:G:G 3707/3708, NC_000022.10:19955156:G:T 1/3708)

- Oct 12, 2018 (152)
86 ALFA NC_000022.11 - 19967634 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
ss292736330, ss481860336, ss1699291938, ss1713731254, ss3643334861 NC_000022.9:18335156:G:A NC_000022.11:19967633:G:A (self)
80217684, 31357186, 5869223, 19773940, 17108175, 20826354, 42273850, 11291545, 90010021, ss238022318, ss481893104, ss482853184, ss485724506, ss537584024, ss778634790, ss783307921, ss784260093, ss832569336, ss834092448, ss995222837, ss1366683250, ss1429219798, ss1579704284, ss1639754012, ss1682748045, ss1752413986, ss1938784432, ss2030165236, ss2158775191, ss2413284211, ss2633862792, ss2972986684, ss2985850733, ss3019086418, ss3352776510, ss3628506032, ss3631815179, ss3633268870, ss3633984261, ss3634860959, ss3635668897, ss3636556593, ss3637421091, ss3638374453, ss3640568260, ss3685618938, ss3743823310, ss3745160790, ss3759230967, ss3772656773, ss3825965524, ss3835927819, ss3841592413, ss3890256870, ss4017873662, ss5232040714 NC_000022.10:19955156:G:A NC_000022.11:19967633:G:A (self)
566544851, 2227954, 237444198, 380218176, 5008904557, ss2246457313, ss3028920334, ss3374061991, ss3707955024, ss3822398855, ss3847107073, ss5105109229 NC_000022.11:19967633:G:A NC_000022.11:19967633:G:A (self)
ss12673788, ss13346918, ss16926321, ss66862098, ss75253638, ss119588336, ss160974848, ss174802312 NT_011519.10:3107306:G:A NC_000022.11:19967633:G:A (self)
ss1639754013, ss1682748046 NC_000022.10:19955156:G:T NC_000022.11:19967633:G:T (self)
ss2246457313 NC_000022.11:19967633:G:T NC_000022.11:19967633:G:T (self)
Help

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

1 citation for rs9306235
PMID Title Author Year Journal
20551675 Localizing putative markers in genetic association studies by incorporating linkage disequilibrium into bayesian hierarchical models. Fridley BL et al. 2010 Human heredity
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.post676+237644a