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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.

rs6481595

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr10:29471722 (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
T>A / T>C / T>G
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.270135 (71502/264690, TOPMED)
G=0.263108 (36842/140026, GnomAD)
T=0.48963 (13836/28258, 14KJPN) (+ 18 more)
G=0.25278 (4775/18890, ALFA)
T=0.49075 (8225/16760, 8.3KJPN)
G=0.3468 (2221/6404, 1000G_30x)
G=0.3510 (1758/5008, 1000G)
G=0.2812 (1260/4480, Estonian)
G=0.2340 (902/3854, ALSPAC)
G=0.2290 (849/3708, TWINSUK)
T=0.4539 (1330/2930, KOREAN)
T=0.4405 (807/1832, Korea1K)
G=0.251 (250/998, GoNL)
G=0.253 (152/600, NorthernSweden)
G=0.271 (89/328, HapMap)
T=0.360 (111/308, SGDP_PRJ)
G=0.181 (39/216, Qatari)
T=0.434 (92/212, Vietnamese)
G=0.07 (6/88, Ancient Sardinia)
G=0.20 (8/40, GENOME_DK)
T=0.33 (12/36, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
SVIL-AS1 : Intron Variant
SVIL : 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 18890 T=0.74722 G=0.25278
European Sub 14286 T=0.76074 G=0.23926
African Sub 2946 T=0.7346 G=0.2654
African Others Sub 114 T=0.754 G=0.246
African American Sub 2832 T=0.7338 G=0.2662
Asian Sub 112 T=0.438 G=0.562
East Asian Sub 86 T=0.43 G=0.57
Other Asian Sub 26 T=0.46 G=0.54
Latin American 1 Sub 146 T=0.651 G=0.349
Latin American 2 Sub 610 T=0.623 G=0.377
South Asian Sub 98 T=0.57 G=0.43
Other Sub 692 T=0.727 G=0.273


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 T=0.729865 G=0.270135
gnomAD - Genomes Global Study-wide 140026 T=0.736892 G=0.263108
gnomAD - Genomes European Sub 75844 T=0.75982 G=0.24018
gnomAD - Genomes African Sub 41952 T=0.73320 G=0.26680
gnomAD - Genomes American Sub 13636 T=0.66691 G=0.33309
gnomAD - Genomes Ashkenazi Jewish Sub 3322 T=0.8221 G=0.1779
gnomAD - Genomes East Asian Sub 3120 T=0.4535 G=0.5465
gnomAD - Genomes Other Sub 2152 T=0.7235 G=0.2765
14KJPN JAPANESE Study-wide 28258 T=0.48963 G=0.51037
Allele Frequency Aggregator Total Global 18890 T=0.74722 G=0.25278
Allele Frequency Aggregator European Sub 14286 T=0.76074 G=0.23926
Allele Frequency Aggregator African Sub 2946 T=0.7346 G=0.2654
Allele Frequency Aggregator Other Sub 692 T=0.727 G=0.273
Allele Frequency Aggregator Latin American 2 Sub 610 T=0.623 G=0.377
Allele Frequency Aggregator Latin American 1 Sub 146 T=0.651 G=0.349
Allele Frequency Aggregator Asian Sub 112 T=0.438 G=0.562
Allele Frequency Aggregator South Asian Sub 98 T=0.57 G=0.43
8.3KJPN JAPANESE Study-wide 16760 T=0.49075 G=0.50925
1000Genomes_30x Global Study-wide 6404 T=0.6532 G=0.3468
1000Genomes_30x African Sub 1786 T=0.7475 G=0.2525
1000Genomes_30x Europe Sub 1266 T=0.7567 G=0.2433
1000Genomes_30x South Asian Sub 1202 T=0.6373 G=0.3627
1000Genomes_30x East Asian Sub 1170 T=0.4436 G=0.5564
1000Genomes_30x American Sub 980 T=0.617 G=0.383
1000Genomes Global Study-wide 5008 T=0.6490 G=0.3510
1000Genomes African Sub 1322 T=0.7466 G=0.2534
1000Genomes East Asian Sub 1008 T=0.4425 G=0.5575
1000Genomes Europe Sub 1006 T=0.7535 G=0.2465
1000Genomes South Asian Sub 978 T=0.638 G=0.362
1000Genomes American Sub 694 T=0.627 G=0.373
Genetic variation in the Estonian population Estonian Study-wide 4480 T=0.7188 G=0.2812
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 T=0.7660 G=0.2340
UK 10K study - Twins TWIN COHORT Study-wide 3708 T=0.7710 G=0.2290
KOREAN population from KRGDB KOREAN Study-wide 2930 T=0.4539 A=0.0000, C=0.0000, G=0.5461
Korean Genome Project KOREAN Study-wide 1832 T=0.4405 G=0.5595
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 T=0.749 G=0.251
Northern Sweden ACPOP Study-wide 600 T=0.747 G=0.253
HapMap Global Study-wide 328 T=0.729 G=0.271
HapMap African Sub 120 T=0.800 G=0.200
HapMap American Sub 120 T=0.792 G=0.208
HapMap Asian Sub 88 T=0.55 G=0.45
SGDP_PRJ Global Study-wide 308 T=0.360 G=0.640
Qatari Global Study-wide 216 T=0.819 G=0.181
A Vietnamese Genetic Variation Database Global Study-wide 212 T=0.434 G=0.566
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 88 T=0.93 G=0.07
The Danish reference pan genome Danish Study-wide 40 T=0.80 G=0.20
Siberian Global Study-wide 36 T=0.33 G=0.67
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 10 NC_000010.11:g.29471722T>A
GRCh38.p14 chr 10 NC_000010.11:g.29471722T>C
GRCh38.p14 chr 10 NC_000010.11:g.29471722T>G
GRCh37.p13 chr 10 NC_000010.10:g.29760651T>A
GRCh37.p13 chr 10 NC_000010.10:g.29760651T>C
GRCh37.p13 chr 10 NC_000010.10:g.29760651T>G
SVIL RefSeqGene NG_033998.1:g.269080A>T
SVIL RefSeqGene NG_033998.1:g.269080A>G
SVIL RefSeqGene NG_033998.1:g.269080A>C
Gene: SVIL, supervillin (minus strand)
Molecule type Change Amino acid[Codon] SO Term
SVIL transcript variant 3 NM_001323599.2:c.4600-479…

NM_001323599.2:c.4600-479A>T

 		N/A Intron Variant
SVIL transcript variant 4 NM_001323600.1:c.4348-479…

NM_001323600.1:c.4348-479A>T

 		N/A Intron Variant
SVIL transcript variant 1 NM_003174.3:c.4252-479A>T N/A Intron Variant
SVIL transcript variant 2 NM_021738.3:c.5530-479A>T N/A Intron Variant
Gene: SVIL-AS1, SVIL antisense RNA 1 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
SVIL-AS1 transcript variant 1 NR_110920.1:n. N/A Intron Variant
SVIL-AS1 transcript variant 2 NR_110921.1:n. N/A Intron Variant
SVIL-AS1 transcript variant 3 NR_110922.1:n. N/A Intron Variant
SVIL-AS1 transcript variant 9 NR_110927.1:n. N/A Intron Variant
SVIL-AS1 transcript variant 6 NR_003930.2:n. N/A Genic Downstream Transcript Variant
SVIL-AS1 transcript variant 4 NR_110923.1:n. N/A Genic Downstream Transcript Variant
SVIL-AS1 transcript variant 5 NR_110924.1:n. N/A Genic Downstream Transcript Variant
SVIL-AS1 transcript variant 7 NR_110925.1:n. N/A Genic Downstream Transcript Variant
SVIL-AS1 transcript variant 8 NR_110926.1:n. N/A Genic Downstream Transcript Variant
SVIL-AS1 transcript variant 10 NR_110928.1:n. N/A Genic Downstream Transcript Variant
SVIL-AS1 transcript variant 11 NR_110929.1: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 T= A C G
GRCh38.p14 chr 10 NC_000010.11:g.29471722= NC_000010.11:g.29471722T>A NC_000010.11:g.29471722T>C NC_000010.11:g.29471722T>G
GRCh37.p13 chr 10 NC_000010.10:g.29760651= NC_000010.10:g.29760651T>A NC_000010.10:g.29760651T>C NC_000010.10:g.29760651T>G
SVIL RefSeqGene NG_033998.1:g.269080= NG_033998.1:g.269080A>T NG_033998.1:g.269080A>G NG_033998.1:g.269080A>C
SVIL transcript variant 3 NM_001323599.2:c.4600-479= NM_001323599.2:c.4600-479A>T NM_001323599.2:c.4600-479A>G NM_001323599.2:c.4600-479A>C
SVIL transcript variant 4 NM_001323600.1:c.4348-479= NM_001323600.1:c.4348-479A>T NM_001323600.1:c.4348-479A>G NM_001323600.1:c.4348-479A>C
SVIL transcript variant 1 NM_003174.3:c.4252-479= NM_003174.3:c.4252-479A>T NM_003174.3:c.4252-479A>G NM_003174.3:c.4252-479A>C
SVIL transcript variant 2 NM_021738.2:c.5530-479= NM_021738.2:c.5530-479A>T NM_021738.2:c.5530-479A>G NM_021738.2:c.5530-479A>C
SVIL transcript variant 2 NM_021738.3:c.5530-479= NM_021738.3:c.5530-479A>T NM_021738.3:c.5530-479A>G NM_021738.3:c.5530-479A>C
SVIL transcript variant X1 XM_005252564.1:c.5890-479= XM_005252564.1:c.5890-479A>T XM_005252564.1:c.5890-479A>G XM_005252564.1:c.5890-479A>C
SVIL transcript variant X2 XM_005252565.1:c.5812-479= XM_005252565.1:c.5812-479A>T XM_005252565.1:c.5812-479A>G XM_005252565.1:c.5812-479A>C
SVIL transcript variant X3 XM_005252566.1:c.5794-479= XM_005252566.1:c.5794-479A>T XM_005252566.1:c.5794-479A>G XM_005252566.1:c.5794-479A>C
SVIL transcript variant X4 XM_005252567.1:c.5764-479= XM_005252567.1:c.5764-479A>T XM_005252567.1:c.5764-479A>G XM_005252567.1:c.5764-479A>C
SVIL transcript variant X5 XM_005252568.1:c.5719-479= XM_005252568.1:c.5719-479A>T XM_005252568.1:c.5719-479A>G XM_005252568.1:c.5719-479A>C
SVIL transcript variant X6 XM_005252569.1:c.5668-479= XM_005252569.1:c.5668-479A>T XM_005252569.1:c.5668-479A>G XM_005252569.1:c.5668-479A>C
SVIL transcript variant X7 XM_005252570.1:c.5656-479= XM_005252570.1:c.5656-479A>T XM_005252570.1:c.5656-479A>G XM_005252570.1:c.5656-479A>C
SVIL transcript variant X8 XM_005252571.1:c.5656-479= XM_005252571.1:c.5656-479A>T XM_005252571.1:c.5656-479A>G XM_005252571.1:c.5656-479A>C
SVIL transcript variant X9 XM_005252572.1:c.5656-479= XM_005252572.1:c.5656-479A>T XM_005252572.1:c.5656-479A>G XM_005252572.1:c.5656-479A>C
SVIL transcript variant X10 XM_005252573.1:c.5656-479= XM_005252573.1:c.5656-479A>T XM_005252573.1:c.5656-479A>G XM_005252573.1:c.5656-479A>C
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#.

65 SubSNP, 21 Frequency submissions
No Submitter Submission ID Date (Build)
1 BCM_SSAHASNP ss10581381 Jul 11, 2003 (116)
2 WI_SSAHASNP ss12058846 Jul 11, 2003 (116)
3 SC_SNP ss15775349 Feb 27, 2004 (120)
4 PERLEGEN ss24203492 Sep 20, 2004 (123)
5 HGSV ss77751238 Dec 07, 2007 (129)
6 BCMHGSC_JDW ss88145568 Mar 23, 2008 (129)
7 BGI ss106666553 Feb 05, 2009 (130)
8 ENSEMBL ss131761908 Dec 01, 2009 (131)
9 GMI ss154773618 Dec 01, 2009 (131)
10 COMPLETE_GENOMICS ss168111903 Jul 04, 2010 (132)
11 BUSHMAN ss201333708 Jul 04, 2010 (132)
12 1000GENOMES ss224649547 Jul 14, 2010 (132)
13 1000GENOMES ss235117127 Jul 15, 2010 (132)
14 1000GENOMES ss241836910 Jul 15, 2010 (132)
15 GMI ss280541027 May 04, 2012 (137)
16 PJP ss291005605 May 09, 2011 (134)
17 TISHKOFF ss561868898 Apr 25, 2013 (138)
18 SSMP ss656491573 Apr 25, 2013 (138)
19 EVA-GONL ss987343487 Aug 21, 2014 (142)
20 JMKIDD_LAB ss1076879438 Aug 21, 2014 (142)
21 1000GENOMES ss1336850557 Aug 21, 2014 (142)
22 DDI ss1426268836 Apr 01, 2015 (144)
23 EVA_GENOME_DK ss1575014526 Apr 01, 2015 (144)
24 EVA_DECODE ss1597006813 Apr 01, 2015 (144)
25 EVA_UK10K_ALSPAC ss1624290759 Apr 01, 2015 (144)
26 EVA_UK10K_TWINSUK ss1667284792 Apr 01, 2015 (144)
27 HAMMER_LAB ss1806327031 Sep 08, 2015 (146)
28 WEILL_CORNELL_DGM ss1930677918 Feb 12, 2016 (147)
29 GENOMED ss1967094658 Jul 19, 2016 (147)
30 JJLAB ss2026068225 Sep 14, 2016 (149)
31 USC_VALOUEV ss2154315187 Dec 20, 2016 (150)
32 HUMAN_LONGEVITY ss2173804660 Dec 20, 2016 (150)
33 SYSTEMSBIOZJU ss2627504624 Nov 08, 2017 (151)
34 GRF ss2698548521 Nov 08, 2017 (151)
35 GNOMAD ss2887114395 Nov 08, 2017 (151)
36 SWEGEN ss3006179182 Nov 08, 2017 (151)
37 BIOINF_KMB_FNS_UNIBA ss3026821237 Nov 08, 2017 (151)
38 CSHL ss3349034868 Nov 08, 2017 (151)
39 URBANLAB ss3649326329 Oct 12, 2018 (152)
40 EGCUT_WGS ss3673699851 Jul 13, 2019 (153)
41 EVA_DECODE ss3689575238 Jul 13, 2019 (153)
42 ACPOP ss3737193290 Jul 13, 2019 (153)
43 EVA ss3747927449 Jul 13, 2019 (153)
44 KHV_HUMAN_GENOMES ss3813291587 Jul 13, 2019 (153)
45 EVA ss3832047883 Apr 26, 2020 (154)
46 EVA ss3839556317 Apr 26, 2020 (154)
47 EVA ss3845023750 Apr 26, 2020 (154)
48 SGDP_PRJ ss3873849055 Apr 26, 2020 (154)
49 KRGDB ss3921822191 Apr 26, 2020 (154)
50 KOGIC ss3967481180 Apr 26, 2020 (154)
51 EVA ss3985467628 Apr 26, 2021 (155)
52 TOPMED ss4847263297 Apr 26, 2021 (155)
53 TOMMO_GENOMICS ss5196918445 Apr 26, 2021 (155)
54 1000G_HIGH_COVERAGE ss5283436989 Oct 16, 2022 (156)
55 EVA ss5392508001 Oct 16, 2022 (156)
56 HUGCELL_USP ss5479156983 Oct 16, 2022 (156)
57 EVA ss5509956158 Oct 16, 2022 (156)
58 1000G_HIGH_COVERAGE ss5577064812 Oct 16, 2022 (156)
59 SANFORD_IMAGENETICS ss5648972654 Oct 16, 2022 (156)
60 TOMMO_GENOMICS ss5741960456 Oct 16, 2022 (156)
61 YY_MCH ss5811331293 Oct 16, 2022 (156)
62 EVA ss5824182223 Oct 16, 2022 (156)
63 EVA ss5849504679 Oct 16, 2022 (156)
64 EVA ss5878318493 Oct 16, 2022 (156)
65 EVA ss5940265968 Oct 16, 2022 (156)
66 1000Genomes NC_000010.10 - 29760651 Oct 12, 2018 (152)
67 1000Genomes_30x NC_000010.11 - 29471722 Oct 16, 2022 (156)
68 The Avon Longitudinal Study of Parents and Children NC_000010.10 - 29760651 Oct 12, 2018 (152)
69 Genetic variation in the Estonian population NC_000010.10 - 29760651 Oct 12, 2018 (152)
70 The Danish reference pan genome NC_000010.10 - 29760651 Apr 26, 2020 (154)
71 gnomAD - Genomes NC_000010.11 - 29471722 Apr 26, 2021 (155)
72 Genome of the Netherlands Release 5 NC_000010.10 - 29760651 Apr 26, 2020 (154)
73 HapMap NC_000010.11 - 29471722 Apr 26, 2020 (154)
74 KOREAN population from KRGDB NC_000010.10 - 29760651 Apr 26, 2020 (154)
75 Korean Genome Project NC_000010.11 - 29471722 Apr 26, 2020 (154)
76 Northern Sweden NC_000010.10 - 29760651 Jul 13, 2019 (153)
77 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000010.10 - 29760651 Apr 26, 2021 (155)
78 Qatari NC_000010.10 - 29760651 Apr 26, 2020 (154)
79 SGDP_PRJ NC_000010.10 - 29760651 Apr 26, 2020 (154)
80 Siberian NC_000010.10 - 29760651 Apr 26, 2020 (154)
81 8.3KJPN NC_000010.10 - 29760651 Apr 26, 2021 (155)
82 14KJPN NC_000010.11 - 29471722 Oct 16, 2022 (156)
83 TopMed NC_000010.11 - 29471722 Apr 26, 2021 (155)
84 UK 10K study - Twins NC_000010.10 - 29760651 Oct 12, 2018 (152)
85 A Vietnamese Genetic Variation Database NC_000010.10 - 29760651 Jul 13, 2019 (153)
86 ALFA NC_000010.11 - 29471722 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)
rs17834535 Oct 08, 2004 (123)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
28999585, ss3921822191 NC_000010.10:29760650:T:A NC_000010.11:29471721:T:A (self)
28999585, ss3921822191 NC_000010.10:29760650:T:C NC_000010.11:29471721:T:C (self)
ss77751238 NC_000010.8:29800656:T:G NC_000010.11:29471721:T:G (self)
ss88145568, ss168111903, ss201333708, ss280541027, ss291005605, ss1597006813 NC_000010.9:29800656:T:G NC_000010.11:29471721:T:G (self)
49218018, 27349423, 19438099, 2094557, 12193064, 28999585, 10478155, 693555, 12719848, 25866035, 6831541, 54887752, 27349423, 6073691, ss224649547, ss235117127, ss241836910, ss561868898, ss656491573, ss987343487, ss1076879438, ss1336850557, ss1426268836, ss1575014526, ss1624290759, ss1667284792, ss1806327031, ss1930677918, ss1967094658, ss2026068225, ss2154315187, ss2627504624, ss2698548521, ss2887114395, ss3006179182, ss3349034868, ss3673699851, ss3737193290, ss3747927449, ss3832047883, ss3839556317, ss3873849055, ss3921822191, ss3985467628, ss5196918445, ss5392508001, ss5509956158, ss5648972654, ss5824182223, ss5940265968 NC_000010.10:29760650:T:G NC_000010.11:29471721:T:G (self)
64590747, 347532645, 372078, 23859181, 75797560, 62808952, 7669525724, ss2173804660, ss3026821237, ss3649326329, ss3689575238, ss3813291587, ss3845023750, ss3967481180, ss4847263297, ss5283436989, ss5479156983, ss5577064812, ss5741960456, ss5811331293, ss5849504679, ss5878318493 NC_000010.11:29471721:T:G NC_000010.11:29471721:T:G (self)
ss10581381, ss12058846 NT_008705.14:11735975:T:G NC_000010.11:29471721:T:G (self)
ss15775349 NT_008705.15:11735975:T:G NC_000010.11:29471721:T:G (self)
ss24203492, ss106666553, ss131761908, ss154773618 NT_008705.16:29700650:T:G NC_000010.11:29471721:T:G (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 rs6481595

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