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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.

rs28126

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr5:65629243 (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
G=0.390313 (103312/264690, TOPMED)
G=0.377224 (52760/139864, GnomAD)
G=0.37165 (20141/54194, ALFA) (+ 17 more)
A=0.43563 (12310/28258, 14KJPN)
A=0.43538 (7297/16760, 8.3KJPN)
G=0.4211 (2697/6404, 1000G_30x)
G=0.4237 (2122/5008, 1000G)
G=0.3940 (1765/4480, Estonian)
G=0.3438 (1325/3854, ALSPAC)
G=0.3290 (1220/3708, TWINSUK)
A=0.4324 (1267/2930, KOREAN)
A=0.4416 (809/1832, Korea1K)
G=0.4272 (763/1786, HapMap)
G=0.352 (351/998, GoNL)
G=0.297 (178/600, NorthernSweden)
G=0.307 (135/440, SGDP_PRJ)
G=0.417 (90/216, Qatari)
A=0.357 (75/210, Vietnamese)
G=0.27 (14/52, Siberian)
G=0.30 (12/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
SHLD3 : Intron Variant
TRAPPC13 : 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 54194 G=0.37165 A=0.62835
European Sub 38812 G=0.36089 A=0.63911
African Sub 6772 G=0.3808 A=0.6192
African Others Sub 226 G=0.425 A=0.575
African American Sub 6546 G=0.3793 A=0.6207
Asian Sub 496 G=0.573 A=0.427
East Asian Sub 398 G=0.585 A=0.415
Other Asian Sub 98 G=0.52 A=0.48
Latin American 1 Sub 682 G=0.378 A=0.622
Latin American 2 Sub 3054 G=0.4659 A=0.5341
South Asian Sub 174 G=0.276 A=0.724
Other Sub 4204 G=0.3668 A=0.6332


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=0.390313 A=0.609687
gnomAD - Genomes Global Study-wide 139864 G=0.377224 A=0.622776
gnomAD - Genomes European Sub 75778 G=0.35583 A=0.64417
gnomAD - Genomes African Sub 41882 G=0.36978 A=0.63022
gnomAD - Genomes American Sub 13620 G=0.46057 A=0.53943
gnomAD - Genomes Ashkenazi Jewish Sub 3320 G=0.4148 A=0.5852
gnomAD - Genomes East Asian Sub 3116 G=0.5632 A=0.4368
gnomAD - Genomes Other Sub 2148 G=0.4209 A=0.5791
Allele Frequency Aggregator Total Global 54194 G=0.37165 A=0.62835
Allele Frequency Aggregator European Sub 38812 G=0.36089 A=0.63911
Allele Frequency Aggregator African Sub 6772 G=0.3808 A=0.6192
Allele Frequency Aggregator Other Sub 4204 G=0.3668 A=0.6332
Allele Frequency Aggregator Latin American 2 Sub 3054 G=0.4659 A=0.5341
Allele Frequency Aggregator Latin American 1 Sub 682 G=0.378 A=0.622
Allele Frequency Aggregator Asian Sub 496 G=0.573 A=0.427
Allele Frequency Aggregator South Asian Sub 174 G=0.276 A=0.724
14KJPN JAPANESE Study-wide 28258 G=0.56437 A=0.43563
8.3KJPN JAPANESE Study-wide 16760 G=0.56462 A=0.43538
1000Genomes_30x Global Study-wide 6404 G=0.4211 A=0.5789
1000Genomes_30x African Sub 1786 G=0.3757 A=0.6243
1000Genomes_30x Europe Sub 1266 G=0.3712 A=0.6288
1000Genomes_30x South Asian Sub 1202 G=0.3286 A=0.6714
1000Genomes_30x East Asian Sub 1170 G=0.5778 A=0.4222
1000Genomes_30x American Sub 980 G=0.495 A=0.505
1000Genomes Global Study-wide 5008 G=0.4237 A=0.5763
1000Genomes African Sub 1322 G=0.3767 A=0.6233
1000Genomes East Asian Sub 1008 G=0.5784 A=0.4216
1000Genomes Europe Sub 1006 G=0.3807 A=0.6193
1000Genomes South Asian Sub 978 G=0.324 A=0.676
1000Genomes American Sub 694 G=0.491 A=0.509
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.3940 A=0.6060
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.3438 A=0.6562
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.3290 A=0.6710
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.5676 A=0.4324
Korean Genome Project KOREAN Study-wide 1832 G=0.5584 A=0.4416
HapMap Global Study-wide 1786 G=0.4272 A=0.5728
HapMap African Sub 692 G=0.392 A=0.608
HapMap American Sub 668 G=0.385 A=0.615
HapMap Asian Sub 250 G=0.636 A=0.364
HapMap Europe Sub 176 G=0.432 A=0.568
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.352 A=0.648
Northern Sweden ACPOP Study-wide 600 G=0.297 A=0.703
SGDP_PRJ Global Study-wide 440 G=0.307 A=0.693
Qatari Global Study-wide 216 G=0.417 A=0.583
A Vietnamese Genetic Variation Database Global Study-wide 210 G=0.643 A=0.357
Siberian Global Study-wide 52 G=0.27 A=0.73
The Danish reference pan genome Danish Study-wide 40 G=0.30 A=0.70
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 5 NC_000005.10:g.65629243G>A
GRCh37.p13 chr 5 NC_000005.9:g.64925070G>A
Gene: TRAPPC13, trafficking protein particle complex subunit 13 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
TRAPPC13 transcript variant 1 NM_001093755.2:c.46+4137G…

NM_001093755.2:c.46+4137G>A

 		N/A Intron Variant
TRAPPC13 transcript variant 3 NM_001093756.2:c.46+4137G…

NM_001093756.2:c.46+4137G>A

 		N/A Intron Variant
TRAPPC13 transcript variant 5 NM_001243737.2:c.46+4137G…

NM_001243737.2:c.46+4137G>A

 		N/A Intron Variant
TRAPPC13 transcript variant 6 NM_001365342.1:c.-341+413…

NM_001365342.1:c.-341+4137G>A

 		N/A Intron Variant
TRAPPC13 transcript variant 7 NM_001365343.1:c.-341+413…

NM_001365343.1:c.-341+4137G>A

 		N/A Intron Variant
TRAPPC13 transcript variant 2 NM_024941.4:c.46+4137G>A N/A Intron Variant
Gene: SHLD3, shieldin complex subunit 3 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
SHLD3 transcript NM_001365341.2:c.-120-225…

NM_001365341.2:c.-120-225G>A

 		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 G= A
GRCh38.p14 chr 5 NC_000005.10:g.65629243= NC_000005.10:g.65629243G>A
GRCh37.p13 chr 5 NC_000005.9:g.64925070= NC_000005.9:g.64925070G>A
LOC643079 transcript NM_001039896.1:c.-345= NM_001039896.1:c.-345G>A
TRAPPC13 transcript variant 1 NM_001093755.1:c.46+4137= NM_001093755.1:c.46+4137G>A
TRAPPC13 transcript variant 1 NM_001093755.2:c.46+4137= NM_001093755.2:c.46+4137G>A
TRAPPC13 transcript variant 3 NM_001093756.1:c.46+4137= NM_001093756.1:c.46+4137G>A
TRAPPC13 transcript variant 3 NM_001093756.2:c.46+4137= NM_001093756.2:c.46+4137G>A
TRAPPC13 transcript variant 5 NM_001243737.1:c.46+4137= NM_001243737.1:c.46+4137G>A
TRAPPC13 transcript variant 5 NM_001243737.2:c.46+4137= NM_001243737.2:c.46+4137G>A
SHLD3 transcript NM_001365341.2:c.-120-225= NM_001365341.2:c.-120-225G>A
TRAPPC13 transcript variant 6 NM_001365342.1:c.-341+4137= NM_001365342.1:c.-341+4137G>A
TRAPPC13 transcript variant 7 NM_001365343.1:c.-341+4137= NM_001365343.1:c.-341+4137G>A
TRAPPC13 transcript variant 2 NM_024941.3:c.46+4137= NM_024941.3:c.46+4137G>A
TRAPPC13 transcript variant 2 NM_024941.4:c.46+4137= NM_024941.4:c.46+4137G>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#.

105 SubSNP, 20 Frequency submissions
No Submitter Submission ID Date (Build)
1 KWOK ss49157 May 08, 2000 (76)
2 KWOK ss49164 May 08, 2000 (76)
3 KWOK ss339007 Jul 10, 2000 (79)
4 KWOK ss339499 Jul 10, 2000 (79)
5 KWOK ss944347 Oct 04, 2000 (86)
6 KWOK ss1059459 Oct 04, 2000 (86)
7 KWOK ss1059479 Oct 04, 2000 (86)
8 KWOK ss1760922 Oct 18, 2000 (92)
9 KWOK ss1855376 Oct 18, 2000 (92)
10 KWOK ss1855387 Oct 18, 2000 (92)
11 SC_JCM ss3570952 Sep 28, 2001 (100)
12 CSHL-HAPMAP ss17072631 Feb 27, 2004 (120)
13 CSHL-HAPMAP ss17847625 Feb 27, 2004 (120)
14 SSAHASNP ss22217987 Apr 05, 2004 (121)
15 PERLEGEN ss23899156 Sep 20, 2004 (123)
16 ABI ss44600754 Mar 14, 2006 (126)
17 ILLUMINA ss65738410 Oct 16, 2006 (127)
18 AFFY ss66136448 Dec 01, 2006 (127)
19 ILLUMINA ss74908083 Dec 07, 2007 (129)
20 AFFY ss76148951 Dec 07, 2007 (129)
21 KRIBB_YJKIM ss81404931 Dec 15, 2007 (130)
22 BCMHGSC_JDW ss93122214 Mar 24, 2008 (129)
23 HUMANGENOME_JCVI ss98729657 Feb 06, 2009 (130)
24 1000GENOMES ss109094760 Jan 23, 2009 (130)
25 1000GENOMES ss111945730 Jan 25, 2009 (130)
26 ILLUMINA-UK ss116644458 Feb 14, 2009 (130)
27 ENSEMBL ss139467090 Dec 01, 2009 (131)
28 ENSEMBL ss143187313 Dec 01, 2009 (131)
29 GMI ss155530038 Dec 01, 2009 (131)
30 ILLUMINA ss160581265 Dec 01, 2009 (131)
31 COMPLETE_GENOMICS ss162321664 Jul 04, 2010 (132)
32 COMPLETE_GENOMICS ss165121379 Jul 04, 2010 (132)
33 COMPLETE_GENOMICS ss166633629 Jul 04, 2010 (132)
34 AFFY ss172643838 Jul 04, 2010 (132)
35 ILLUMINA ss173471148 Jul 04, 2010 (132)
36 BUSHMAN ss200337502 Jul 04, 2010 (132)
37 BCM-HGSC-SUB ss207206160 Jul 04, 2010 (132)
38 1000GENOMES ss221717201 Jul 14, 2010 (132)
39 1000GENOMES ss232974416 Jul 14, 2010 (132)
40 1000GENOMES ss240140665 Jul 15, 2010 (132)
41 BL ss253506855 May 09, 2011 (134)
42 GMI ss278319191 May 04, 2012 (137)
43 GMI ss285190660 Apr 25, 2013 (138)
44 PJP ss293371755 May 09, 2011 (134)
45 ILLUMINA ss410925983 Sep 17, 2011 (135)
46 ILLUMINA ss481539213 Sep 08, 2015 (146)
47 ILLUMINA ss537129125 Sep 08, 2015 (146)
48 TISHKOFF ss558436259 Apr 25, 2013 (138)
49 SSMP ss652306516 Apr 25, 2013 (138)
50 EVA-GONL ss981642748 Aug 21, 2014 (142)
51 JMKIDD_LAB ss1072686828 Aug 21, 2014 (142)
52 1000GENOMES ss1315391282 Aug 21, 2014 (142)
53 DDI ss1430366299 Apr 01, 2015 (144)
54 EVA_GENOME_DK ss1581167408 Apr 01, 2015 (144)
55 EVA_DECODE ss1591161444 Apr 01, 2015 (144)
56 EVA_UK10K_ALSPAC ss1613044003 Apr 01, 2015 (144)
57 EVA_UK10K_TWINSUK ss1656038036 Apr 01, 2015 (144)
58 EVA_SVP ss1712769155 Apr 01, 2015 (144)
59 HAMMER_LAB ss1803611399 Sep 08, 2015 (146)
60 WEILL_CORNELL_DGM ss1924897698 Feb 12, 2016 (147)
61 GENOMED ss1970104484 Jul 19, 2016 (147)
62 JJLAB ss2023054232 Sep 14, 2016 (149)
63 USC_VALOUEV ss2151210026 Dec 20, 2016 (150)
64 HUMAN_LONGEVITY ss2274311989 Dec 20, 2016 (150)
65 SYSTEMSBIOZJU ss2626023600 Nov 08, 2017 (151)
66 GRF ss2706754894 Nov 08, 2017 (151)
67 GNOMAD ss2825449051 Nov 08, 2017 (151)
68 SWEGEN ss2997051790 Nov 08, 2017 (151)
69 BIOINF_KMB_FNS_UNIBA ss3025311661 Nov 08, 2017 (151)
70 CSHL ss3346420493 Nov 08, 2017 (151)
71 ILLUMINA ss3629249415 Oct 12, 2018 (152)
72 ILLUMINA ss3636716333 Oct 12, 2018 (152)
73 ILLUMINA ss3638557244 Oct 12, 2018 (152)
74 ILLUMINA ss3643502867 Oct 12, 2018 (152)
75 URBANLAB ss3648076793 Oct 12, 2018 (152)
76 EGCUT_WGS ss3664934237 Jul 13, 2019 (153)
77 EVA_DECODE ss3714826246 Jul 13, 2019 (153)
78 ACPOP ss3732419214 Jul 13, 2019 (153)
79 EVA ss3763519083 Jul 13, 2019 (153)
80 PACBIO ss3785130040 Jul 13, 2019 (153)
81 PACBIO ss3790533405 Jul 13, 2019 (153)
82 PACBIO ss3795410078 Jul 13, 2019 (153)
83 KHV_HUMAN_GENOMES ss3806686664 Jul 13, 2019 (153)
84 EVA ss3829280483 Apr 26, 2020 (154)
85 EVA ss3838113140 Apr 26, 2020 (154)
86 EVA ss3843553933 Apr 26, 2020 (154)
87 SGDP_PRJ ss3862004408 Apr 26, 2020 (154)
88 KRGDB ss3908557931 Apr 26, 2020 (154)
89 KOGIC ss3956823167 Apr 26, 2020 (154)
90 EVA ss4017210136 Apr 26, 2021 (155)
91 TOPMED ss4662548492 Apr 26, 2021 (155)
92 TOMMO_GENOMICS ss5172070048 Apr 26, 2021 (155)
93 1000G_HIGH_COVERAGE ss5264229882 Oct 17, 2022 (156)
94 EVA ss5358038534 Oct 17, 2022 (156)
95 HUGCELL_USP ss5462384491 Oct 17, 2022 (156)
96 EVA ss5508051382 Oct 17, 2022 (156)
97 1000G_HIGH_COVERAGE ss5548016084 Oct 17, 2022 (156)
98 SANFORD_IMAGENETICS ss5637951214 Oct 17, 2022 (156)
99 TOMMO_GENOMICS ss5708559590 Oct 17, 2022 (156)
100 YY_MCH ss5806383236 Oct 17, 2022 (156)
101 EVA ss5835025624 Oct 17, 2022 (156)
102 EVA ss5854842172 Oct 17, 2022 (156)
103 EVA ss5894480663 Oct 17, 2022 (156)
104 EVA ss5966381403 Oct 17, 2022 (156)
105 EVA ss5980297606 Oct 17, 2022 (156)
106 1000Genomes NC_000005.9 - 64925070 Oct 12, 2018 (152)
107 1000Genomes_30x NC_000005.10 - 65629243 Oct 17, 2022 (156)
108 The Avon Longitudinal Study of Parents and Children NC_000005.9 - 64925070 Oct 12, 2018 (152)
109 Genetic variation in the Estonian population NC_000005.9 - 64925070 Oct 12, 2018 (152)
110 The Danish reference pan genome NC_000005.9 - 64925070 Apr 26, 2020 (154)
111 gnomAD - Genomes NC_000005.10 - 65629243 Apr 26, 2021 (155)
112 Genome of the Netherlands Release 5 NC_000005.9 - 64925070 Apr 26, 2020 (154)
113 HapMap NC_000005.10 - 65629243 Apr 26, 2020 (154)
114 KOREAN population from KRGDB NC_000005.9 - 64925070 Apr 26, 2020 (154)
115 Korean Genome Project NC_000005.10 - 65629243 Apr 26, 2020 (154)
116 Northern Sweden NC_000005.9 - 64925070 Jul 13, 2019 (153)
117 Qatari NC_000005.9 - 64925070 Apr 26, 2020 (154)
118 SGDP_PRJ NC_000005.9 - 64925070 Apr 26, 2020 (154)
119 Siberian NC_000005.9 - 64925070 Apr 26, 2020 (154)
120 8.3KJPN NC_000005.9 - 64925070 Apr 26, 2021 (155)
121 14KJPN NC_000005.10 - 65629243 Oct 17, 2022 (156)
122 TopMed NC_000005.10 - 65629243 Apr 26, 2021 (155)
123 UK 10K study - Twins NC_000005.9 - 64925070 Oct 12, 2018 (152)
124 A Vietnamese Genetic Variation Database NC_000005.9 - 64925070 Jul 13, 2019 (153)
125 ALFA NC_000005.10 - 65629243 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).

Associated ID History Updated (Build)
rs1301348 Jan 18, 2001 (92)
rs60231055 Feb 27, 2009 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss93122214, ss109094760, ss111945730, ss116644458, ss162321664, ss165121379, ss166633629, ss200337502, ss207206160, ss253506855, ss278319191, ss285190660, ss293371755, ss1591161444, ss1712769155, ss3643502867 NC_000005.8:64960825:G:A NC_000005.10:65629242:G:A (self)
27001549, 15010943, 10672485, 7332347, 6674055, 15735325, 5704079, 6939628, 14021388, 3726380, 30039355, 15010943, 3333760, ss221717201, ss232974416, ss240140665, ss481539213, ss537129125, ss558436259, ss652306516, ss981642748, ss1072686828, ss1315391282, ss1430366299, ss1581167408, ss1613044003, ss1656038036, ss1803611399, ss1924897698, ss1970104484, ss2023054232, ss2151210026, ss2626023600, ss2706754894, ss2825449051, ss2997051790, ss3346420493, ss3629249415, ss3636716333, ss3638557244, ss3664934237, ss3732419214, ss3763519083, ss3785130040, ss3790533405, ss3795410078, ss3829280483, ss3838113140, ss3862004408, ss3908557931, ss4017210136, ss5172070048, ss5358038534, ss5508051382, ss5637951214, ss5835025624, ss5966381403, ss5980297606 NC_000005.9:64925069:G:A NC_000005.10:65629242:G:A (self)
35542019, 190821946, 2880853, 13201168, 42396694, 499926049, 3094768337, ss2274311989, ss3025311661, ss3648076793, ss3714826246, ss3806686664, ss3843553933, ss3956823167, ss4662548492, ss5264229882, ss5462384491, ss5548016084, ss5708559590, ss5806383236, ss5854842172, ss5894480663 NC_000005.10:65629242:G:A NC_000005.10:65629242:G:A (self)
ss17072631, ss17847625, ss22217987 NT_006431.13:15489811:G:A NC_000005.10:65629242:G:A (self)
ss49157, ss49164, ss339007, ss339499, ss944347, ss1059459, ss1059479, ss1760922, ss1855376, ss1855387, ss3570952, ss23899156, ss44600754, ss65738410, ss66136448, ss74908083, ss76148951, ss81404931, ss98729657, ss139467090, ss143187313, ss155530038, ss160581265, ss172643838, ss173471148, ss410925983 NT_006713.15:15519428:G:A NC_000005.10:65629242: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 rs28126

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