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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.

rs7013055

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr8:55560249 (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>C / A>G
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.446859 (118279/264690, TOPMED)
G=0.431612 (60335/139790, GnomAD)
G=0.36766 (23401/63648, ALFA) (+ 20 more)
G=0.44515 (12579/28258, 14KJPN)
G=0.44666 (7486/16760, 8.3KJPN)
G=0.4775 (3058/6404, 1000G_30x)
G=0.4772 (2390/5008, 1000G)
G=0.3467 (1553/4480, Estonian)
G=0.3887 (1498/3854, ALSPAC)
G=0.3878 (1438/3708, TWINSUK)
G=0.4611 (1351/2930, KOREAN)
A=0.4679 (975/2084, HGDP_Stanford)
G=0.4793 (904/1886, HapMap)
G=0.4563 (836/1832, Korea1K)
G=0.4167 (470/1128, Daghestan)
G=0.386 (385/998, GoNL)
G=0.350 (210/600, NorthernSweden)
A=0.287 (113/394, SGDP_PRJ)
G=0.449 (97/216, Qatari)
A=0.471 (99/210, Vietnamese)
G=0.26 (18/70, Ancient Sardinia)
G=0.40 (16/40, GENOME_DK)
A=0.41 (13/32, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
None
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: 20231103111315
Population Group Sample Size Ref Allele Alt Allele Ref HMOZ Alt HMOZ HTRZ HWEP
Total Global 63648 A=0.63234 C=0.00000, G=0.36766 0.410665 0.14599 0.443345 N/A
European Sub 54028 A=0.64409 C=0.00000, G=0.35591 0.422559 0.134375 0.443067 17
African Sub 2608 A=0.6093 C=0.0000, G=0.3907 0.409509 0.190951 0.39954 18
African Others Sub 100 A=0.50 C=0.00, G=0.50 0.32 0.32 0.36 3
African American Sub 2508 A=0.6136 C=0.0000, G=0.3864 0.413078 0.185805 0.401116 16
Asian Sub 106 A=0.613 C=0.000, G=0.387 0.433962 0.207547 0.358491 2
East Asian Sub 82 A=0.63 C=0.00, G=0.37 0.463415 0.195122 0.341463 2
Other Asian Sub 24 A=0.54 C=0.00, G=0.46 0.333333 0.25 0.416667 0
Latin American 1 Sub 158 A=0.715 C=0.000, G=0.285 0.556962 0.126582 0.316456 3
Latin American 2 Sub 748 A=0.561 C=0.000, G=0.439 0.360963 0.237968 0.40107 8
South Asian Sub 4886 A=0.5237 C=0.0000, G=0.4763 0.279574 0.232092 0.488334 1
Other Sub 1114 A=0.6302 C=0.0000, G=0.3698 0.421903 0.16158 0.416517 4


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=0.553141 G=0.446859
gnomAD - Genomes Global Study-wide 139790 A=0.568388 G=0.431612
gnomAD - Genomes European Sub 75730 A=0.62571 G=0.37429
gnomAD - Genomes African Sub 41840 A=0.49089 G=0.50911
gnomAD - Genomes American Sub 13634 A=0.50000 G=0.50000
gnomAD - Genomes Ashkenazi Jewish Sub 3318 A=0.6245 G=0.3755
gnomAD - Genomes East Asian Sub 3118 A=0.4541 G=0.5459
gnomAD - Genomes Other Sub 2150 A=0.5702 G=0.4298
Allele Frequency Aggregator Total Global 63648 A=0.63234 C=0.00000, G=0.36766
Allele Frequency Aggregator European Sub 54028 A=0.64409 C=0.00000, G=0.35591
Allele Frequency Aggregator South Asian Sub 4886 A=0.5237 C=0.0000, G=0.4763
Allele Frequency Aggregator African Sub 2608 A=0.6093 C=0.0000, G=0.3907
Allele Frequency Aggregator Other Sub 1114 A=0.6302 C=0.0000, G=0.3698
Allele Frequency Aggregator Latin American 2 Sub 748 A=0.561 C=0.000, G=0.439
Allele Frequency Aggregator Latin American 1 Sub 158 A=0.715 C=0.000, G=0.285
Allele Frequency Aggregator Asian Sub 106 A=0.613 C=0.000, G=0.387
14KJPN JAPANESE Study-wide 28258 A=0.55485 G=0.44515
8.3KJPN JAPANESE Study-wide 16760 A=0.55334 G=0.44666
1000Genomes_30x Global Study-wide 6404 A=0.5225 G=0.4775
1000Genomes_30x African Sub 1786 A=0.4776 G=0.5224
1000Genomes_30x Europe Sub 1266 A=0.6556 G=0.3444
1000Genomes_30x South Asian Sub 1202 A=0.5191 G=0.4809
1000Genomes_30x East Asian Sub 1170 A=0.4846 G=0.5154
1000Genomes_30x American Sub 980 A=0.482 G=0.518
1000Genomes Global Study-wide 5008 A=0.5228 G=0.4772
1000Genomes African Sub 1322 A=0.4781 G=0.5219
1000Genomes East Asian Sub 1008 A=0.4911 G=0.5089
1000Genomes Europe Sub 1006 A=0.6491 G=0.3509
1000Genomes South Asian Sub 978 A=0.517 G=0.483
1000Genomes American Sub 694 A=0.478 G=0.522
Genetic variation in the Estonian population Estonian Study-wide 4480 A=0.6533 G=0.3467
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 A=0.6113 G=0.3887
UK 10K study - Twins TWIN COHORT Study-wide 3708 A=0.6122 G=0.3878
KOREAN population from KRGDB KOREAN Study-wide 2930 A=0.5389 G=0.4611
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 A=0.4679 G=0.5321
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 A=0.472 G=0.528
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 A=0.420 G=0.580
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 A=0.597 G=0.403
HGDP-CEPH-db Supplement 1 Europe Sub 320 A=0.641 G=0.359
HGDP-CEPH-db Supplement 1 Africa Sub 242 A=0.326 G=0.674
HGDP-CEPH-db Supplement 1 America Sub 216 A=0.190 G=0.810
HGDP-CEPH-db Supplement 1 Oceania Sub 72 A=0.62 G=0.38
HapMap Global Study-wide 1886 A=0.5207 G=0.4793
HapMap American Sub 768 A=0.533 G=0.467
HapMap African Sub 688 A=0.461 G=0.539
HapMap Asian Sub 254 A=0.567 G=0.433
HapMap Europe Sub 176 A=0.636 G=0.364
Korean Genome Project KOREAN Study-wide 1832 A=0.5437 G=0.4563
Genome-wide autozygosity in Daghestan Global Study-wide 1128 A=0.5833 G=0.4167
Genome-wide autozygosity in Daghestan Daghestan Sub 622 A=0.619 G=0.381
Genome-wide autozygosity in Daghestan Near_East Sub 144 A=0.514 G=0.486
Genome-wide autozygosity in Daghestan Central Asia Sub 122 A=0.500 G=0.500
Genome-wide autozygosity in Daghestan Europe Sub 108 A=0.593 G=0.407
Genome-wide autozygosity in Daghestan South Asian Sub 96 A=0.57 G=0.43
Genome-wide autozygosity in Daghestan Caucasus Sub 36 A=0.53 G=0.47
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 A=0.614 G=0.386
Northern Sweden ACPOP Study-wide 600 A=0.650 G=0.350
SGDP_PRJ Global Study-wide 394 A=0.287 G=0.713
Qatari Global Study-wide 216 A=0.551 G=0.449
A Vietnamese Genetic Variation Database Global Study-wide 210 A=0.471 G=0.529
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 70 A=0.74 G=0.26
The Danish reference pan genome Danish Study-wide 40 A=0.60 G=0.40
Siberian Global Study-wide 32 A=0.41 G=0.59
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 8 NC_000008.11:g.55560249A>C
GRCh38.p14 chr 8 NC_000008.11:g.55560249A>G
GRCh37.p13 chr 8 NC_000008.10:g.56472808A>C
GRCh37.p13 chr 8 NC_000008.10:g.56472808A>G
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= C G
GRCh38.p14 chr 8 NC_000008.11:g.55560249= NC_000008.11:g.55560249A>C NC_000008.11:g.55560249A>G
GRCh37.p13 chr 8 NC_000008.10:g.56472808= NC_000008.10:g.56472808A>C NC_000008.10:g.56472808A>G
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#.

99 SubSNP, 23 Frequency submissions
No Submitter Submission ID Date (Build)
1 BCM_SSAHASNP ss10480266 Jul 11, 2003 (116)
2 ABI ss43301726 Mar 14, 2006 (126)
3 ILLUMINA ss66816995 Nov 30, 2006 (127)
4 ILLUMINA ss67529693 Nov 30, 2006 (127)
5 ILLUMINA ss67898475 Nov 30, 2006 (127)
6 ILLUMINA ss70902470 May 24, 2008 (130)
7 ILLUMINA ss71498092 May 17, 2007 (127)
8 ILLUMINA ss75815587 Dec 06, 2007 (129)
9 ILLUMINA ss79242504 Dec 14, 2007 (130)
10 KRIBB_YJKIM ss84597612 Dec 14, 2007 (130)
11 BCMHGSC_JDW ss93890110 Mar 25, 2008 (129)
12 HUMANGENOME_JCVI ss98074638 Feb 04, 2009 (130)
13 BGI ss105619308 Feb 04, 2009 (130)
14 1000GENOMES ss108036982 Jan 22, 2009 (130)
15 1000GENOMES ss115419215 Jan 25, 2009 (130)
16 ILLUMINA-UK ss115952655 Feb 14, 2009 (130)
17 ILLUMINA ss122670098 Dec 01, 2009 (131)
18 ENSEMBL ss133501460 Dec 01, 2009 (131)
19 ENSEMBL ss143484441 Dec 01, 2009 (131)
20 ILLUMINA ss154398561 Dec 01, 2009 (131)
21 ILLUMINA ss159573932 Dec 01, 2009 (131)
22 COMPLETE_GENOMICS ss162418848 Jul 04, 2010 (132)
23 COMPLETE_GENOMICS ss164700665 Jul 04, 2010 (132)
24 COMPLETE_GENOMICS ss166653585 Jul 04, 2010 (132)
25 ILLUMINA ss172232967 Jul 04, 2010 (132)
26 ILLUMINA ss174205677 Jul 04, 2010 (132)
27 BUSHMAN ss199180554 Jul 04, 2010 (132)
28 BCM-HGSC-SUB ss206516272 Jul 04, 2010 (132)
29 1000GENOMES ss223712601 Jul 14, 2010 (132)
30 1000GENOMES ss234442901 Jul 15, 2010 (132)
31 1000GENOMES ss241298313 Jul 15, 2010 (132)
32 BL ss254345382 May 09, 2011 (134)
33 GMI ss279817744 May 04, 2012 (137)
34 GMI ss285846540 Apr 25, 2013 (138)
35 PJP ss294085047 May 09, 2011 (134)
36 ILLUMINA ss537422666 Sep 08, 2015 (146)
37 TISHKOFF ss560757575 Apr 25, 2013 (138)
38 SSMP ss655194718 Apr 25, 2013 (138)
39 ILLUMINA ss825573022 Apr 01, 2015 (144)
40 ILLUMINA ss833085023 Jul 13, 2019 (153)
41 EVA-GONL ss985532349 Aug 21, 2014 (142)
42 JMKIDD_LAB ss1075531681 Aug 21, 2014 (142)
43 1000GENOMES ss1329926848 Aug 21, 2014 (142)
44 HAMMER_LAB ss1397525924 Sep 08, 2015 (146)
45 DDI ss1431516595 Apr 01, 2015 (144)
46 EVA_GENOME_DK ss1582689723 Apr 01, 2015 (144)
47 EVA_DECODE ss1595128057 Apr 01, 2015 (144)
48 EVA_UK10K_ALSPAC ss1620674105 Apr 01, 2015 (144)
49 EVA_UK10K_TWINSUK ss1663668138 Apr 01, 2015 (144)
50 EVA_SVP ss1713037231 Apr 01, 2015 (144)
51 HAMMER_LAB ss1805541070 Sep 08, 2015 (146)
52 WEILL_CORNELL_DGM ss1928819807 Feb 12, 2016 (147)
53 GENOMED ss1970983095 Jul 19, 2016 (147)
54 JJLAB ss2025110357 Sep 14, 2016 (149)
55 USC_VALOUEV ss2153336777 Dec 20, 2016 (150)
56 HUMAN_LONGEVITY ss2303247861 Dec 20, 2016 (150)
57 SYSTEMSBIOZJU ss2627036090 Nov 08, 2017 (151)
58 GRF ss2709105724 Nov 08, 2017 (151)
59 GNOMAD ss2866985390 Nov 08, 2017 (151)
60 SWEGEN ss3003210686 Nov 08, 2017 (151)
61 BIOINF_KMB_FNS_UNIBA ss3026342013 Nov 08, 2017 (151)
62 CSHL ss3348188072 Nov 08, 2017 (151)
63 ILLUMINA ss3630062718 Oct 12, 2018 (152)
64 ILLUMINA ss3638760839 Oct 12, 2018 (152)
65 ILLUMINA ss3639382665 Oct 12, 2018 (152)
66 ILLUMINA ss3639720502 Oct 12, 2018 (152)
67 ILLUMINA ss3643691658 Oct 12, 2018 (152)
68 URBANLAB ss3648919218 Oct 12, 2018 (152)
69 EGCUT_WGS ss3670888797 Jul 13, 2019 (153)
70 EVA_DECODE ss3722051025 Jul 13, 2019 (153)
71 ACPOP ss3735677489 Jul 13, 2019 (153)
72 EVA ss3768022554 Jul 13, 2019 (153)
73 PACBIO ss3786150442 Jul 13, 2019 (153)
74 PACBIO ss3791405683 Jul 13, 2019 (153)
75 PACBIO ss3796287025 Jul 13, 2019 (153)
76 KHV_HUMAN_GENOMES ss3811178878 Jul 13, 2019 (153)
77 EVA ss3831171697 Apr 26, 2020 (154)
78 EVA ss3839094979 Apr 26, 2020 (154)
79 EVA ss3844554409 Apr 26, 2020 (154)
80 HGDP ss3847913921 Apr 26, 2020 (154)
81 SGDP_PRJ ss3869963538 Apr 26, 2020 (154)
82 KRGDB ss3917472263 Apr 26, 2020 (154)
83 KOGIC ss3963911512 Apr 26, 2020 (154)
84 EVA ss3985360616 Apr 26, 2021 (155)
85 EVA ss4017390883 Apr 26, 2021 (155)
86 TOPMED ss4786777007 Apr 26, 2021 (155)
87 TOMMO_GENOMICS ss5188792622 Apr 26, 2021 (155)
88 1000G_HIGH_COVERAGE ss5277205082 Oct 14, 2022 (156)
89 EVA ss5381269793 Oct 14, 2022 (156)
90 HUGCELL_USP ss5473765892 Oct 14, 2022 (156)
91 EVA ss5509359653 Oct 14, 2022 (156)
92 1000G_HIGH_COVERAGE ss5567608560 Oct 14, 2022 (156)
93 SANFORD_IMAGENETICS ss5645415071 Oct 14, 2022 (156)
94 TOMMO_GENOMICS ss5730881842 Oct 14, 2022 (156)
95 YY_MCH ss5809725895 Oct 14, 2022 (156)
96 EVA ss5830557900 Oct 14, 2022 (156)
97 EVA ss5856381020 Oct 14, 2022 (156)
98 EVA ss5889036232 Oct 14, 2022 (156)
99 EVA ss5974623161 Oct 14, 2022 (156)
100 1000Genomes NC_000008.10 - 56472808 Oct 12, 2018 (152)
101 1000Genomes_30x NC_000008.11 - 55560249 Oct 14, 2022 (156)
102 The Avon Longitudinal Study of Parents and Children NC_000008.10 - 56472808 Oct 12, 2018 (152)
103 Genome-wide autozygosity in Daghestan NC_000008.9 - 56635362 Apr 26, 2020 (154)
104 Genetic variation in the Estonian population NC_000008.10 - 56472808 Oct 12, 2018 (152)
105 The Danish reference pan genome NC_000008.10 - 56472808 Apr 26, 2020 (154)
106 gnomAD - Genomes NC_000008.11 - 55560249 Apr 26, 2021 (155)
107 Genome of the Netherlands Release 5 NC_000008.10 - 56472808 Apr 26, 2020 (154)
108 HGDP-CEPH-db Supplement 1 NC_000008.9 - 56635362 Apr 26, 2020 (154)
109 HapMap NC_000008.11 - 55560249 Apr 26, 2020 (154)
110 KOREAN population from KRGDB NC_000008.10 - 56472808 Apr 26, 2020 (154)
111 Korean Genome Project NC_000008.11 - 55560249 Apr 26, 2020 (154)
112 Northern Sweden NC_000008.10 - 56472808 Jul 13, 2019 (153)
113 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000008.10 - 56472808 Apr 26, 2021 (155)
114 Qatari NC_000008.10 - 56472808 Apr 26, 2020 (154)
115 SGDP_PRJ NC_000008.10 - 56472808 Apr 26, 2020 (154)
116 Siberian NC_000008.10 - 56472808 Apr 26, 2020 (154)
117 8.3KJPN NC_000008.10 - 56472808 Apr 26, 2021 (155)
118 14KJPN NC_000008.11 - 55560249 Oct 14, 2022 (156)
119 TopMed NC_000008.11 - 55560249 Apr 26, 2021 (155)
120 UK 10K study - Twins NC_000008.10 - 56472808 Oct 12, 2018 (152)
121 A Vietnamese Genetic Variation Database NC_000008.10 - 56472808 Jul 13, 2019 (153)
122 ALFA NC_000008.11 - 55560249 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)
rs57942315 May 24, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
2505149927 NC_000008.11:55560248:A:C NC_000008.11:55560248:A:C (self)
499758, 591813, ss93890110, ss108036982, ss115419215, ss115952655, ss162418848, ss164700665, ss166653585, ss199180554, ss206516272, ss254345382, ss279817744, ss285846540, ss294085047, ss825573022, ss1397525924, ss1595128057, ss1713037231, ss3639382665, ss3639720502, ss3643691658, ss3847913921 NC_000008.9:56635361:A:G NC_000008.11:55560248:A:G (self)
42053541, 23386251, 16627045, 8854661, 10440226, 24649657, 8962354, 586543, 10861737, 21980518, 5853131, 46761929, 23386251, 5203607, ss223712601, ss234442901, ss241298313, ss537422666, ss560757575, ss655194718, ss833085023, ss985532349, ss1075531681, ss1329926848, ss1431516595, ss1582689723, ss1620674105, ss1663668138, ss1805541070, ss1928819807, ss1970983095, ss2025110357, ss2153336777, ss2627036090, ss2709105724, ss2866985390, ss3003210686, ss3348188072, ss3630062718, ss3638760839, ss3670888797, ss3735677489, ss3768022554, ss3786150442, ss3791405683, ss3796287025, ss3831171697, ss3839094979, ss3869963538, ss3917472263, ss3985360616, ss4017390883, ss5188792622, ss5381269793, ss5509359653, ss5645415071, ss5830557900, ss5974623161 NC_000008.10:56472807:A:G NC_000008.11:55560248:A:G (self)
55134495, 296554937, 3626092, 20289513, 64718946, 624154567, 2505149927, ss2303247861, ss3026342013, ss3648919218, ss3722051025, ss3811178878, ss3844554409, ss3963911512, ss4786777007, ss5277205082, ss5473765892, ss5567608560, ss5730881842, ss5809725895, ss5856381020, ss5889036232 NC_000008.11:55560248:A:G NC_000008.11:55560248:A:G (self)
ss10480266 NT_008183.16:8315356:A:G NC_000008.11:55560248:A:G (self)
ss43301726, ss66816995, ss67529693, ss67898475, ss70902470, ss71498092, ss75815587, ss79242504, ss84597612, ss98074638, ss105619308, ss122670098, ss133501460, ss143484441, ss154398561, ss159573932, ss172232967, ss174205677 NT_008183.19:8337208:A:G NC_000008.11:55560248:A: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 rs7013055

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.post820+afb47a3d