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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.

rs2795116

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr9:73158245 (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
A>G / A>T
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.132102 (34966/264690, TOPMED)
G=0.095872 (14598/152266, ALFA)
G=0.129804 (18186/140104, GnomAD) (+ 21 more)
G=0.20642 (5833/28258, 14KJPN)
G=0.20883 (3500/16760, 8.3KJPN)
G=0.1540 (986/6404, 1000G_30x)
G=0.1496 (749/5008, 1000G)
G=0.0942 (422/4480, Estonian)
G=0.0823 (317/3854, ALSPAC)
G=0.0868 (322/3708, TWINSUK)
G=0.2539 (744/2930, KOREAN)
G=0.1494 (311/2082, HGDP_Stanford)
G=0.1644 (311/1892, HapMap)
G=0.2462 (451/1832, Korea1K)
G=0.1261 (143/1134, Daghestan)
G=0.098 (98/998, GoNL)
G=0.112 (67/600, NorthernSweden)
G=0.083 (18/216, Qatari)
G=0.107 (23/214, Vietnamese)
A=0.447 (76/170, SGDP_PRJ)
G=0.03 (2/58, Ancient Sardinia)
G=0.05 (2/40, GENOME_DK)
A=0.50 (11/22, Siberian)
G=0.50 (11/22, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
ANXA1 : Intron 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 152266 A=0.904128 G=0.095872
European Sub 128748 A=0.915191 G=0.084809
African Sub 9312 A=0.7718 G=0.2282
African Others Sub 326 A=0.745 G=0.255
African American Sub 8986 A=0.7728 G=0.2272
Asian Sub 632 A=0.821 G=0.179
East Asian Sub 500 A=0.810 G=0.190
Other Asian Sub 132 A=0.864 G=0.136
Latin American 1 Sub 752 A=0.904 G=0.096
Latin American 2 Sub 6332 A=0.9010 G=0.0990
South Asian Sub 186 A=0.823 G=0.177
Other Sub 6304 A=0.8875 G=0.1125


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 A=0.867898 G=0.132102
Allele Frequency Aggregator Total Global 152266 A=0.904128 G=0.095872
Allele Frequency Aggregator European Sub 128748 A=0.915191 G=0.084809
Allele Frequency Aggregator African Sub 9312 A=0.7718 G=0.2282
Allele Frequency Aggregator Latin American 2 Sub 6332 A=0.9010 G=0.0990
Allele Frequency Aggregator Other Sub 6304 A=0.8875 G=0.1125
Allele Frequency Aggregator Latin American 1 Sub 752 A=0.904 G=0.096
Allele Frequency Aggregator Asian Sub 632 A=0.821 G=0.179
Allele Frequency Aggregator South Asian Sub 186 A=0.823 G=0.177
gnomAD - Genomes Global Study-wide 140104 A=0.870196 G=0.129804
gnomAD - Genomes European Sub 75904 A=0.91165 G=0.08835
gnomAD - Genomes African Sub 41956 A=0.77755 G=0.22245
gnomAD - Genomes American Sub 13646 A=0.92555 G=0.07445
gnomAD - Genomes Ashkenazi Jewish Sub 3318 A=0.9002 G=0.0998
gnomAD - Genomes East Asian Sub 3128 A=0.8251 G=0.1749
gnomAD - Genomes Other Sub 2152 A=0.8824 G=0.1176
14KJPN JAPANESE Study-wide 28258 A=0.79358 G=0.20642
8.3KJPN JAPANESE Study-wide 16760 A=0.79117 G=0.20883
1000Genomes_30x Global Study-wide 6404 A=0.8460 G=0.1540
1000Genomes_30x African Sub 1786 A=0.7609 G=0.2391
1000Genomes_30x Europe Sub 1266 A=0.9021 G=0.0979
1000Genomes_30x South Asian Sub 1202 A=0.8561 G=0.1439
1000Genomes_30x East Asian Sub 1170 A=0.8556 G=0.1444
1000Genomes_30x American Sub 980 A=0.905 G=0.095
1000Genomes Global Study-wide 5008 A=0.8504 G=0.1496
1000Genomes African Sub 1322 A=0.7700 G=0.2300
1000Genomes East Asian Sub 1008 A=0.8542 G=0.1458
1000Genomes Europe Sub 1006 A=0.9026 G=0.0974
1000Genomes South Asian Sub 978 A=0.861 G=0.139
1000Genomes American Sub 694 A=0.908 G=0.092
Genetic variation in the Estonian population Estonian Study-wide 4480 A=0.9058 G=0.0942
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 A=0.9177 G=0.0823
UK 10K study - Twins TWIN COHORT Study-wide 3708 A=0.9132 G=0.0868
KOREAN population from KRGDB KOREAN Study-wide 2930 A=0.7461 G=0.2539
HGDP-CEPH-db Supplement 1 Global Study-wide 2082 A=0.8506 G=0.1494
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 A=0.804 G=0.196
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 A=0.836 G=0.164
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 A=0.871 G=0.129
HGDP-CEPH-db Supplement 1 Europe Sub 320 A=0.912 G=0.087
HGDP-CEPH-db Supplement 1 Africa Sub 240 A=0.733 G=0.267
HGDP-CEPH-db Supplement 1 America Sub 216 A=0.954 G=0.046
HGDP-CEPH-db Supplement 1 Oceania Sub 72 A=0.94 G=0.06
HapMap Global Study-wide 1892 A=0.8356 G=0.1644
HapMap American Sub 770 A=0.869 G=0.131
HapMap African Sub 692 A=0.775 G=0.225
HapMap Asian Sub 254 A=0.850 G=0.150
HapMap Europe Sub 176 A=0.909 G=0.091
Korean Genome Project KOREAN Study-wide 1832 A=0.7538 G=0.2462
Genome-wide autozygosity in Daghestan Global Study-wide 1134 A=0.8739 G=0.1261
Genome-wide autozygosity in Daghestan Daghestan Sub 628 A=0.873 G=0.127
Genome-wide autozygosity in Daghestan Near_East Sub 144 A=0.847 G=0.153
Genome-wide autozygosity in Daghestan Central Asia Sub 122 A=0.852 G=0.148
Genome-wide autozygosity in Daghestan Europe Sub 108 A=0.926 G=0.074
Genome-wide autozygosity in Daghestan South Asian Sub 96 A=0.88 G=0.12
Genome-wide autozygosity in Daghestan Caucasus Sub 36 A=0.92 G=0.08
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 A=0.902 G=0.098
Northern Sweden ACPOP Study-wide 600 A=0.888 G=0.112
Qatari Global Study-wide 216 A=0.917 G=0.083
A Vietnamese Genetic Variation Database Global Study-wide 214 A=0.893 G=0.107
SGDP_PRJ Global Study-wide 170 A=0.447 G=0.553
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 58 A=0.97 G=0.03
The Danish reference pan genome Danish Study-wide 40 A=0.95 G=0.05
Siberian Global Study-wide 22 A=0.50 G=0.50
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 9 NC_000009.12:g.73158245A>G
GRCh38.p14 chr 9 NC_000009.12:g.73158245A>T
GRCh37.p13 chr 9 NC_000009.11:g.75773161A>G
GRCh37.p13 chr 9 NC_000009.11:g.75773161A>T
Gene: ANXA1, annexin A1 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
ANXA1 transcript NM_000700.3:c.-14-277A>G N/A Intron Variant
ANXA1 transcript variant X1 XM_017014657.2:c.20-277A>G N/A Intron 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 A= G T
GRCh38.p14 chr 9 NC_000009.12:g.73158245= NC_000009.12:g.73158245A>G NC_000009.12:g.73158245A>T
GRCh37.p13 chr 9 NC_000009.11:g.75773161= NC_000009.11:g.75773161A>G NC_000009.11:g.75773161A>T
ANXA1 transcript NM_000700.1:c.-14-277= NM_000700.1:c.-14-277A>G NM_000700.1:c.-14-277A>T
ANXA1 transcript NM_000700.3:c.-14-277= NM_000700.3:c.-14-277A>G NM_000700.3:c.-14-277A>T
ANXA1 transcript variant X1 XM_005251950.1:c.20-277= XM_005251950.1:c.20-277A>G XM_005251950.1:c.20-277A>T
ANXA1 transcript variant X1 XM_017014657.2:c.20-277= XM_017014657.2:c.20-277A>G XM_017014657.2:c.20-277A>T
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#.

97 SubSNP, 23 Frequency submissions
No Submitter Submission ID Date (Build)
1 SC_JCM ss3958157 Sep 28, 2001 (100)
2 PERLEGEN ss23473019 Sep 20, 2004 (123)
3 SI_EXO ss52076416 Oct 16, 2006 (127)
4 ILLUMINA ss67674540 Nov 30, 2006 (127)
5 ILLUMINA ss71324580 May 17, 2007 (127)
6 ILLUMINA ss75358858 Dec 07, 2007 (129)
7 BCMHGSC_JDW ss94082931 Mar 25, 2008 (129)
8 1000GENOMES ss114538431 Jan 25, 2009 (130)
9 KRIBB_YJKIM ss119445772 Dec 01, 2009 (131)
10 ENSEMBL ss144158280 Dec 01, 2009 (131)
11 GMI ss157576296 Dec 01, 2009 (131)
12 ILLUMINA ss160579435 Dec 01, 2009 (131)
13 COMPLETE_GENOMICS ss164196518 Jul 04, 2010 (132)
14 COMPLETE_GENOMICS ss165159309 Jul 04, 2010 (132)
15 ILLUMINA ss173464610 Jul 04, 2010 (132)
16 1000GENOMES ss224262620 Jul 14, 2010 (132)
17 1000GENOMES ss234829835 Jul 15, 2010 (132)
18 1000GENOMES ss241602807 Jul 15, 2010 (132)
19 GMI ss280259058 May 04, 2012 (137)
20 ILLUMINA ss480664481 May 04, 2012 (137)
21 ILLUMINA ss480679950 May 04, 2012 (137)
22 ILLUMINA ss481531820 Sep 08, 2015 (146)
23 ILLUMINA ss485127156 May 04, 2012 (137)
24 ILLUMINA ss537127055 Sep 08, 2015 (146)
25 TISHKOFF ss561402975 Apr 25, 2013 (138)
26 SSMP ss655889511 Apr 25, 2013 (138)
27 ILLUMINA ss778506460 Aug 21, 2014 (142)
28 ILLUMINA ss783009910 Aug 21, 2014 (142)
29 ILLUMINA ss783970192 Aug 21, 2014 (142)
30 ILLUMINA ss832267235 Apr 01, 2015 (144)
31 ILLUMINA ss833962649 Aug 21, 2014 (142)
32 EVA-GONL ss986599261 Aug 21, 2014 (142)
33 JMKIDD_LAB ss1076325802 Aug 21, 2014 (142)
34 1000GENOMES ss1334030434 Aug 21, 2014 (142)
35 HAMMER_LAB ss1397556590 Sep 08, 2015 (146)
36 EVA_GENOME_DK ss1583111581 Apr 01, 2015 (144)
37 EVA_DECODE ss1596228888 Apr 01, 2015 (144)
38 EVA_UK10K_ALSPAC ss1622797236 Apr 01, 2015 (144)
39 EVA_UK10K_TWINSUK ss1665791269 Apr 01, 2015 (144)
40 EVA_SVP ss1713111520 Apr 01, 2015 (144)
41 ILLUMINA ss1752782021 Sep 08, 2015 (146)
42 HAMMER_LAB ss1805998620 Sep 08, 2015 (146)
43 WEILL_CORNELL_DGM ss1929915302 Feb 12, 2016 (147)
44 GENOMED ss1971222381 Jul 19, 2016 (147)
45 JJLAB ss2025672279 Sep 14, 2016 (149)
46 USC_VALOUEV ss2153896902 Dec 20, 2016 (150)
47 HUMAN_LONGEVITY ss2311520954 Dec 20, 2016 (150)
48 SYSTEMSBIOZJU ss2627303675 Nov 08, 2017 (151)
49 ILLUMINA ss2634870304 Nov 08, 2017 (151)
50 GRF ss2709760712 Nov 08, 2017 (151)
51 GNOMAD ss2879166536 Nov 08, 2017 (151)
52 SWEGEN ss3005008855 Nov 08, 2017 (151)
53 BIOINF_KMB_FNS_UNIBA ss3026617355 Nov 08, 2017 (151)
54 CSHL ss3348689178 Nov 08, 2017 (151)
55 ILLUMINA ss3630272217 Oct 12, 2018 (152)
56 ILLUMINA ss3632762446 Oct 12, 2018 (152)
57 ILLUMINA ss3633534910 Oct 12, 2018 (152)
58 ILLUMINA ss3634263226 Oct 12, 2018 (152)
59 ILLUMINA ss3635215153 Oct 12, 2018 (152)
60 ILLUMINA ss3635941202 Oct 12, 2018 (152)
61 ILLUMINA ss3636962328 Oct 12, 2018 (152)
62 ILLUMINA ss3637694512 Oct 12, 2018 (152)
63 ILLUMINA ss3638815235 Oct 12, 2018 (152)
64 ILLUMINA ss3640922444 Oct 12, 2018 (152)
65 ILLUMINA ss3641242074 Oct 12, 2018 (152)
66 ILLUMINA ss3641540036 Oct 12, 2018 (152)
67 ILLUMINA ss3643741940 Oct 12, 2018 (152)
68 EGCUT_WGS ss3672546073 Jul 13, 2019 (153)
69 EVA_DECODE ss3724046611 Jul 13, 2019 (153)
70 ACPOP ss3736560967 Jul 13, 2019 (153)
71 ILLUMINA ss3745515032 Jul 13, 2019 (153)
72 EVA ss3769245655 Jul 13, 2019 (153)
73 ILLUMINA ss3773007063 Jul 13, 2019 (153)
74 KHV_HUMAN_GENOMES ss3812414911 Jul 13, 2019 (153)
75 EVA ss3825755763 Apr 26, 2020 (154)
76 EVA ss3831676638 Apr 26, 2020 (154)
77 HGDP ss3847949548 Apr 26, 2020 (154)
78 SGDP_PRJ ss3872325749 Apr 26, 2020 (154)
79 KRGDB ss3920115591 Apr 26, 2020 (154)
80 KOGIC ss3966033397 Apr 26, 2020 (154)
81 EVA ss3985421558 Apr 26, 2021 (155)
82 EVA ss4017439701 Apr 26, 2021 (155)
83 TOPMED ss4823036947 Apr 26, 2021 (155)
84 TOMMO_GENOMICS ss5193682018 Apr 26, 2021 (155)
85 1000G_HIGH_COVERAGE ss5280924655 Oct 13, 2022 (156)
86 EVA ss5315404820 Oct 13, 2022 (156)
87 EVA ss5387980300 Oct 13, 2022 (156)
88 HUGCELL_USP ss5476922064 Oct 13, 2022 (156)
89 1000G_HIGH_COVERAGE ss5573354299 Oct 13, 2022 (156)
90 SANFORD_IMAGENETICS ss5647553619 Oct 13, 2022 (156)
91 TOMMO_GENOMICS ss5737734312 Oct 13, 2022 (156)
92 EVA ss5799785229 Oct 13, 2022 (156)
93 YY_MCH ss5810688956 Oct 13, 2022 (156)
94 EVA ss5829253871 Oct 13, 2022 (156)
95 EVA ss5856783343 Oct 13, 2022 (156)
96 EVA ss5916591322 Oct 13, 2022 (156)
97 EVA ss5976731364 Oct 13, 2022 (156)
98 1000Genomes NC_000009.11 - 75773161 Oct 12, 2018 (152)
99 1000Genomes_30x NC_000009.12 - 73158245 Oct 13, 2022 (156)
100 The Avon Longitudinal Study of Parents and Children NC_000009.11 - 75773161 Oct 12, 2018 (152)
101 Genome-wide autozygosity in Daghestan NC_000009.10 - 74962981 Apr 26, 2020 (154)
102 Genetic variation in the Estonian population NC_000009.11 - 75773161 Oct 12, 2018 (152)
103 The Danish reference pan genome NC_000009.11 - 75773161 Apr 26, 2020 (154)
104 gnomAD - Genomes NC_000009.12 - 73158245 Apr 26, 2021 (155)
105 Genome of the Netherlands Release 5 NC_000009.11 - 75773161 Apr 26, 2020 (154)
106 HGDP-CEPH-db Supplement 1 NC_000009.10 - 74962981 Apr 26, 2020 (154)
107 HapMap NC_000009.12 - 73158245 Apr 26, 2020 (154)
108 KOREAN population from KRGDB NC_000009.11 - 75773161 Apr 26, 2020 (154)
109 Korean Genome Project NC_000009.12 - 73158245 Apr 26, 2020 (154)
110 Northern Sweden NC_000009.11 - 75773161 Jul 13, 2019 (153)
111 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000009.11 - 75773161 Apr 26, 2021 (155)
112 Qatari NC_000009.11 - 75773161 Apr 26, 2020 (154)
113 SGDP_PRJ NC_000009.11 - 75773161 Apr 26, 2020 (154)
114 Siberian NC_000009.11 - 75773161 Apr 26, 2020 (154)
115 8.3KJPN NC_000009.11 - 75773161 Apr 26, 2021 (155)
116 14KJPN NC_000009.12 - 73158245 Oct 13, 2022 (156)
117 TopMed NC_000009.12 - 73158245 Apr 26, 2021 (155)
118 UK 10K study - Twins NC_000009.11 - 75773161 Oct 12, 2018 (152)
119 A Vietnamese Genetic Variation Database NC_000009.11 - 75773161 Jul 13, 2019 (153)
120 ALFA NC_000009.12 - 73158245 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
530092, 627440, ss94082931, ss114538431, ss160579435, ss164196518, ss165159309, ss280259058, ss480664481, ss1397556590, ss1596228888, ss1713111520, ss3643741940, ss3847949548 NC_000009.10:74962980:A:G NC_000009.12:73158244:A:G (self)
46296116, 25707132, 18284321, 9276518, 11474654, 27292985, 9845832, 647485, 11957232, 24342729, 6413256, 51651325, 25707132, 5712568, ss224262620, ss234829835, ss241602807, ss480679950, ss481531820, ss485127156, ss537127055, ss561402975, ss655889511, ss778506460, ss783009910, ss783970192, ss832267235, ss833962649, ss986599261, ss1076325802, ss1334030434, ss1583111581, ss1622797236, ss1665791269, ss1752782021, ss1805998620, ss1929915302, ss1971222381, ss2025672279, ss2153896902, ss2627303675, ss2634870304, ss2709760712, ss2879166536, ss3005008855, ss3348689178, ss3630272217, ss3632762446, ss3633534910, ss3634263226, ss3635215153, ss3635941202, ss3636962328, ss3637694512, ss3638815235, ss3640922444, ss3641242074, ss3641540036, ss3672546073, ss3736560967, ss3745515032, ss3769245655, ss3773007063, ss3825755763, ss3831676638, ss3872325749, ss3920115591, ss3985421558, ss4017439701, ss5193682018, ss5315404820, ss5387980300, ss5647553619, ss5799785229, ss5829253871, ss5976731364 NC_000009.11:75773160:A:G NC_000009.12:73158244:A:G (self)
60880234, 327334914, 3837970, 22411398, 71571416, 660414508, 5951122585, ss2311520954, ss3026617355, ss3724046611, ss3812414911, ss3966033397, ss4823036947, ss5280924655, ss5476922064, ss5573354299, ss5737734312, ss5810688956, ss5856783343, ss5916591322 NC_000009.12:73158244:A:G NC_000009.12:73158244:A:G (self)
ss3958157, ss23473019, ss67674540, ss71324580, ss75358858, ss119445772, ss144158280, ss157576296, ss173464610 NT_008470.19:4937692:A:G NC_000009.12:73158244:A:G (self)
ss52076416 NT_023935.17:4937692:A:G NC_000009.12:73158244:A:G (self)
ss2311520954 NC_000009.12:73158244:A:T NC_000009.12:73158244:A:T (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 rs2795116

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