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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.

rs4084127

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr11:69781755 (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 / G>C
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.361474 (101598/281066, ALFA)
A=0.330606 (87508/264690, TOPMED)
A=0.321875 (45058/139986, GnomAD) (+ 20 more)
A=0.30900 (24315/78690, PAGE_STUDY)
A=0.12807 (3619/28258, 14KJPN)
A=0.12698 (2128/16758, 8.3KJPN)
A=0.2970 (1902/6404, 1000G_30x)
A=0.2927 (1466/5008, 1000G)
A=0.3042 (1363/4480, Estonian)
A=0.3768 (1452/3854, ALSPAC)
A=0.3956 (1467/3708, TWINSUK)
A=0.1338 (392/2930, KOREAN)
A=0.2630 (494/1878, HapMap)
A=0.350 (349/998, GoNL)
A=0.157 (124/790, PRJEB37584)
A=0.498 (312/626, Chileans)
A=0.273 (164/600, NorthernSweden)
G=0.352 (102/290, SGDP_PRJ)
A=0.306 (66/216, Qatari)
A=0.255 (55/216, Vietnamese)
A=0.42 (22/52, Ancient Sardinia)
A=0.33 (13/40, GENOME_DK)
G=0.33 (8/24, 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: 20230706150541
Population Group Sample Size Ref Allele Alt Allele
Total Global 286102 G=0.638992 A=0.361008, C=0.000000
European Sub 246956 G=0.634688 A=0.365312, C=0.000000
African Sub 11726 G=0.77853 A=0.22147, C=0.00000
African Others Sub 434 G=0.825 A=0.175, C=0.000
African American Sub 11292 G=0.77674 A=0.22326, C=0.00000
Asian Sub 3894 G=0.8431 A=0.1569, C=0.0000
East Asian Sub 3130 G=0.8665 A=0.1335, C=0.0000
Other Asian Sub 764 G=0.747 A=0.253, C=0.000
Latin American 1 Sub 1174 G=0.6780 A=0.3220, C=0.0000
Latin American 2 Sub 8742 G=0.4800 A=0.5200, C=0.0000
South Asian Sub 376 G=0.713 A=0.287, C=0.000
Other Sub 13234 G=0.63511 A=0.36489, C=0.00000


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
Allele Frequency Aggregator Total Global 281066 G=0.638526 A=0.361474, C=0.000000
Allele Frequency Aggregator European Sub 243862 G=0.634720 A=0.365280, C=0.000000
Allele Frequency Aggregator Other Sub 12434 G=0.63600 A=0.36400, C=0.00000
Allele Frequency Aggregator African Sub 10584 G=0.77787 A=0.22213, C=0.00000
Allele Frequency Aggregator Latin American 2 Sub 8742 G=0.4800 A=0.5200, C=0.0000
Allele Frequency Aggregator Asian Sub 3894 G=0.8431 A=0.1569, C=0.0000
Allele Frequency Aggregator Latin American 1 Sub 1174 G=0.6780 A=0.3220, C=0.0000
Allele Frequency Aggregator South Asian Sub 376 G=0.713 A=0.287, C=0.000
TopMed Global Study-wide 264690 G=0.669394 A=0.330606
gnomAD - Genomes Global Study-wide 139986 G=0.678125 A=0.321875
gnomAD - Genomes European Sub 75816 G=0.64409 A=0.35591
gnomAD - Genomes African Sub 41942 G=0.77283 A=0.22717
gnomAD - Genomes American Sub 13630 G=0.54835 A=0.45165
gnomAD - Genomes Ashkenazi Jewish Sub 3322 G=0.6391 A=0.3609
gnomAD - Genomes East Asian Sub 3124 G=0.8457 A=0.1543
gnomAD - Genomes Other Sub 2152 G=0.6705 A=0.3295
The PAGE Study Global Study-wide 78690 G=0.69100 A=0.30900
The PAGE Study AfricanAmerican Sub 32510 G=0.76303 A=0.23697
The PAGE Study Mexican Sub 10804 G=0.48001 A=0.51999
The PAGE Study Asian Sub 8318 G=0.8438 A=0.1562
The PAGE Study PuertoRican Sub 7918 G=0.6139 A=0.3861
The PAGE Study NativeHawaiian Sub 4534 G=0.7658 A=0.2342
The PAGE Study Cuban Sub 4230 G=0.6381 A=0.3619
The PAGE Study Dominican Sub 3828 G=0.7095 A=0.2905
The PAGE Study CentralAmerican Sub 2450 G=0.5331 A=0.4669
The PAGE Study SouthAmerican Sub 1982 G=0.4561 A=0.5439
The PAGE Study NativeAmerican Sub 1260 G=0.6262 A=0.3738
The PAGE Study SouthAsian Sub 856 G=0.721 A=0.279
14KJPN JAPANESE Study-wide 28258 G=0.87193 A=0.12807
8.3KJPN JAPANESE Study-wide 16758 G=0.87302 A=0.12698
1000Genomes_30x Global Study-wide 6404 G=0.7030 A=0.2970
1000Genomes_30x African Sub 1786 G=0.8180 A=0.1820
1000Genomes_30x Europe Sub 1266 G=0.6398 A=0.3602
1000Genomes_30x South Asian Sub 1202 G=0.6913 A=0.3087
1000Genomes_30x East Asian Sub 1170 G=0.8043 A=0.1957
1000Genomes_30x American Sub 980 G=0.468 A=0.532
1000Genomes Global Study-wide 5008 G=0.7073 A=0.2927
1000Genomes African Sub 1322 G=0.8162 A=0.1838
1000Genomes East Asian Sub 1008 G=0.8085 A=0.1915
1000Genomes Europe Sub 1006 G=0.6471 A=0.3529
1000Genomes South Asian Sub 978 G=0.689 A=0.311
1000Genomes American Sub 694 G=0.465 A=0.535
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.6958 A=0.3042
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.6232 A=0.3768
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.6044 A=0.3956
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.8662 A=0.1338
HapMap Global Study-wide 1878 G=0.7370 A=0.2630
HapMap American Sub 764 G=0.691 A=0.309
HapMap African Sub 688 G=0.789 A=0.211
HapMap Asian Sub 252 G=0.869 A=0.131
HapMap Europe Sub 174 G=0.540 A=0.460
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.650 A=0.350
CNV burdens in cranial meningiomas Global Study-wide 790 G=0.843 A=0.157
CNV burdens in cranial meningiomas CRM Sub 790 G=0.843 A=0.157
Chileans Chilean Study-wide 626 G=0.502 A=0.498
Northern Sweden ACPOP Study-wide 600 G=0.727 A=0.273
SGDP_PRJ Global Study-wide 290 G=0.352 A=0.648
Qatari Global Study-wide 216 G=0.694 A=0.306
A Vietnamese Genetic Variation Database Global Study-wide 216 G=0.745 A=0.255
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 52 G=0.58 A=0.42
The Danish reference pan genome Danish Study-wide 40 G=0.68 A=0.33
Siberian Global Study-wide 24 G=0.33 A=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 11 NC_000011.10:g.69781755G>A
GRCh38.p14 chr 11 NC_000011.10:g.69781755G>C
GRCh37.p13 chr 11 NC_000011.9:g.69596523G>A
GRCh37.p13 chr 11 NC_000011.9:g.69596523G>C
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 C
GRCh38.p14 chr 11 NC_000011.10:g.69781755= NC_000011.10:g.69781755G>A NC_000011.10:g.69781755G>C
GRCh37.p13 chr 11 NC_000011.9:g.69596523= NC_000011.9:g.69596523G>A NC_000011.9:g.69596523G>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#.

115 SubSNP, 23 Frequency submissions
No Submitter Submission ID Date (Build)
1 TSC-CSHL ss5481189 Oct 10, 2002 (108)
2 SC_JCM ss5691569 Feb 20, 2003 (111)
3 SC_SNP ss16146054 Feb 27, 2004 (120)
4 ABI ss38681975 Mar 13, 2006 (126)
5 AFFY ss66431406 Nov 30, 2006 (127)
6 PERLEGEN ss69319818 May 17, 2007 (127)
7 AFFY ss76204565 Dec 06, 2007 (129)
8 KRIBB_YJKIM ss81992626 Dec 15, 2007 (130)
9 BCMHGSC_JDW ss88630219 Mar 23, 2008 (129)
10 1000GENOMES ss114750956 Jan 25, 2009 (130)
11 GMI ss156442737 Dec 01, 2009 (131)
12 ILLUMINA ss160660082 Dec 01, 2009 (131)
13 COMPLETE_GENOMICS ss170170005 Jul 04, 2010 (132)
14 AFFY ss172803382 Jul 04, 2010 (132)
15 ILLUMINA ss173685247 Jul 04, 2010 (132)
16 COMPLETE_GENOMICS ss175175351 Jul 04, 2010 (132)
17 BUSHMAN ss202842492 Jul 04, 2010 (132)
18 BCM-HGSC-SUB ss207622880 Jul 04, 2010 (132)
19 1000GENOMES ss225298242 Jul 14, 2010 (132)
20 1000GENOMES ss235601087 Jul 15, 2010 (132)
21 1000GENOMES ss242224700 Jul 15, 2010 (132)
22 GMI ss281053552 May 04, 2012 (137)
23 GMI ss286402735 Apr 25, 2013 (138)
24 ILLUMINA ss480888884 May 04, 2012 (137)
25 ILLUMINA ss480907693 May 04, 2012 (137)
26 ILLUMINA ss481855019 Sep 08, 2015 (146)
27 ILLUMINA ss485239510 May 04, 2012 (137)
28 ILLUMINA ss537214340 Sep 08, 2015 (146)
29 TISHKOFF ss562631572 Apr 25, 2013 (138)
30 SSMP ss658145642 Apr 25, 2013 (138)
31 ILLUMINA ss778902235 Sep 08, 2015 (146)
32 ILLUMINA ss783065680 Sep 08, 2015 (146)
33 ILLUMINA ss784023622 Sep 08, 2015 (146)
34 ILLUMINA ss832323719 Sep 08, 2015 (146)
35 ILLUMINA ss834363500 Sep 08, 2015 (146)
36 EVA-GONL ss988642342 Aug 21, 2014 (142)
37 JMKIDD_LAB ss1077812314 Aug 21, 2014 (142)
38 1000GENOMES ss1341757015 Aug 21, 2014 (142)
39 DDI ss1426667046 Apr 01, 2015 (144)
40 EVA_GENOME_DK ss1575777647 Apr 01, 2015 (144)
41 EVA_DECODE ss1598304771 Apr 01, 2015 (144)
42 EVA_UK10K_ALSPAC ss1626832629 Apr 01, 2015 (144)
43 EVA_UK10K_TWINSUK ss1669826662 Apr 01, 2015 (144)
44 EVA_SVP ss1713262280 Apr 01, 2015 (144)
45 ILLUMINA ss1752029921 Sep 08, 2015 (146)
46 WEILL_CORNELL_DGM ss1932001628 Feb 12, 2016 (147)
47 ILLUMINA ss1946315169 Feb 12, 2016 (147)
48 ILLUMINA ss1959362085 Feb 12, 2016 (147)
49 GENOMED ss1967385550 Jul 19, 2016 (147)
50 JJLAB ss2026745217 Sep 14, 2016 (149)
51 ILLUMINA ss2095023416 Dec 20, 2016 (150)
52 USC_VALOUEV ss2155053466 Dec 20, 2016 (150)
53 HUMAN_LONGEVITY ss2183304996 Dec 20, 2016 (150)
54 SYSTEMSBIOZJU ss2627846211 Nov 08, 2017 (151)
55 ILLUMINA ss2632847366 Nov 08, 2017 (151)
56 GRF ss2699346017 Nov 08, 2017 (151)
57 ILLUMINA ss2710738743 Nov 08, 2017 (151)
58 GNOMAD ss2901050193 Nov 08, 2017 (151)
59 AFFY ss2985590113 Nov 08, 2017 (151)
60 SWEGEN ss3008293761 Nov 08, 2017 (151)
61 ILLUMINA ss3021349703 Nov 08, 2017 (151)
62 BIOINF_KMB_FNS_UNIBA ss3027170239 Nov 08, 2017 (151)
63 CSHL ss3349653082 Nov 08, 2017 (151)
64 ILLUMINA ss3625603667 Oct 12, 2018 (152)
65 ILLUMINA ss3626683695 Oct 12, 2018 (152)
66 ILLUMINA ss3630863601 Oct 12, 2018 (152)
67 ILLUMINA ss3632989232 Oct 12, 2018 (152)
68 ILLUMINA ss3633688738 Oct 12, 2018 (152)
69 ILLUMINA ss3634461664 Oct 12, 2018 (152)
70 ILLUMINA ss3635380274 Oct 12, 2018 (152)
71 ILLUMINA ss3636144961 Oct 12, 2018 (152)
72 ILLUMINA ss3637131137 Oct 12, 2018 (152)
73 ILLUMINA ss3637913876 Oct 12, 2018 (152)
74 ILLUMINA ss3640169003 Oct 12, 2018 (152)
75 ILLUMINA ss3644567975 Oct 12, 2018 (152)
76 ILLUMINA ss3651714721 Oct 12, 2018 (152)
77 EGCUT_WGS ss3675621394 Jul 13, 2019 (153)
78 EVA_DECODE ss3692019582 Jul 13, 2019 (153)
79 ILLUMINA ss3725252618 Jul 13, 2019 (153)
80 ACPOP ss3738278355 Jul 13, 2019 (153)
81 ILLUMINA ss3744086457 Jul 13, 2019 (153)
82 ILLUMINA ss3744383981 Jul 13, 2019 (153)
83 ILLUMINA ss3744762497 Jul 13, 2019 (153)
84 EVA ss3749442103 Jul 13, 2019 (153)
85 PAGE_CC ss3771633748 Jul 13, 2019 (153)
86 ILLUMINA ss3772262374 Jul 13, 2019 (153)
87 PACBIO ss3786984825 Jul 13, 2019 (153)
88 PACBIO ss3792121009 Jul 13, 2019 (153)
89 PACBIO ss3797003337 Jul 13, 2019 (153)
90 KHV_HUMAN_GENOMES ss3814781307 Jul 13, 2019 (153)
91 EVA ss3832685994 Apr 26, 2020 (154)
92 SGDP_PRJ ss3876507030 Apr 26, 2020 (154)
93 KRGDB ss3924901523 Apr 26, 2020 (154)
94 EVA ss3984652526 Apr 26, 2021 (155)
95 EVA ss3985539399 Apr 26, 2021 (155)
96 TOPMED ss4889460073 Apr 26, 2021 (155)
97 TOMMO_GENOMICS ss5202542420 Apr 26, 2021 (155)
98 1000G_HIGH_COVERAGE ss5287846399 Oct 13, 2022 (156)
99 EVA ss5315553401 Oct 13, 2022 (156)
100 EVA ss5400339574 Oct 13, 2022 (156)
101 HUGCELL_USP ss5482968980 Oct 13, 2022 (156)
102 EVA ss5510402799 Oct 13, 2022 (156)
103 1000G_HIGH_COVERAGE ss5583780341 Oct 13, 2022 (156)
104 SANFORD_IMAGENETICS ss5624277600 Oct 13, 2022 (156)
105 SANFORD_IMAGENETICS ss5651461159 Oct 13, 2022 (156)
106 TOMMO_GENOMICS ss5750599782 Oct 13, 2022 (156)
107 EVA ss5799845700 Oct 13, 2022 (156)
108 YY_MCH ss5812518073 Oct 13, 2022 (156)
109 EVA ss5836823716 Oct 13, 2022 (156)
110 EVA ss5847392716 Oct 13, 2022 (156)
111 EVA ss5847638366 Oct 13, 2022 (156)
112 EVA ss5850023933 Oct 13, 2022 (156)
113 EVA ss5920452679 Oct 13, 2022 (156)
114 EVA ss5942772320 Oct 13, 2022 (156)
115 EVA ss5979362359 Oct 13, 2022 (156)
116 1000Genomes NC_000011.9 - 69596523 Oct 12, 2018 (152)
117 1000Genomes_30x NC_000011.10 - 69781755 Oct 13, 2022 (156)
118 The Avon Longitudinal Study of Parents and Children NC_000011.9 - 69596523 Oct 12, 2018 (152)
119 Chileans NC_000011.9 - 69596523 Apr 26, 2020 (154)
120 Genetic variation in the Estonian population NC_000011.9 - 69596523 Oct 12, 2018 (152)
121 The Danish reference pan genome NC_000011.9 - 69596523 Apr 26, 2020 (154)
122 gnomAD - Genomes NC_000011.10 - 69781755 Apr 26, 2021 (155)
123 Genome of the Netherlands Release 5 NC_000011.9 - 69596523 Apr 26, 2020 (154)
124 HapMap NC_000011.10 - 69781755 Apr 26, 2020 (154)
125 KOREAN population from KRGDB NC_000011.9 - 69596523 Apr 26, 2020 (154)
126 Northern Sweden NC_000011.9 - 69596523 Jul 13, 2019 (153)
127 The PAGE Study NC_000011.10 - 69781755 Jul 13, 2019 (153)
128 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000011.9 - 69596523 Apr 26, 2021 (155)
129 CNV burdens in cranial meningiomas NC_000011.9 - 69596523 Apr 26, 2021 (155)
130 Qatari NC_000011.9 - 69596523 Apr 26, 2020 (154)
131 SGDP_PRJ NC_000011.9 - 69596523 Apr 26, 2020 (154)
132 Siberian NC_000011.9 - 69596523 Apr 26, 2020 (154)
133 8.3KJPN NC_000011.9 - 69596523 Apr 26, 2021 (155)
134 14KJPN NC_000011.10 - 69781755 Oct 13, 2022 (156)
135 TopMed NC_000011.10 - 69781755 Apr 26, 2021 (155)
136 UK 10K study - Twins NC_000011.9 - 69596523 Oct 12, 2018 (152)
137 A Vietnamese Genetic Variation Database NC_000011.9 - 69596523 Jul 13, 2019 (153)
138 ALFA NC_000011.10 - 69781755 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)
rs60433717 Feb 26, 2009 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss88630219, ss114750956, ss170170005, ss175175351, ss202842492, ss207622880, ss281053552, ss286402735, ss480888884, ss1598304771, ss1713262280 NC_000011.8:69305703:G:A NC_000011.10:69781754:G:A (self)
54295842, 30141306, 77539, 21359642, 2612143, 13447502, 32078917, 11563220, 765326, 202004, 14043558, 28524010, 7569820, 60511727, 30141306, 6688034, ss225298242, ss235601087, ss242224700, ss480907693, ss481855019, ss485239510, ss537214340, ss562631572, ss658145642, ss778902235, ss783065680, ss784023622, ss832323719, ss834363500, ss988642342, ss1077812314, ss1341757015, ss1426667046, ss1575777647, ss1626832629, ss1669826662, ss1752029921, ss1932001628, ss1946315169, ss1959362085, ss1967385550, ss2026745217, ss2095023416, ss2155053466, ss2627846211, ss2632847366, ss2699346017, ss2710738743, ss2901050193, ss2985590113, ss3008293761, ss3021349703, ss3349653082, ss3625603667, ss3626683695, ss3630863601, ss3632989232, ss3633688738, ss3634461664, ss3635380274, ss3636144961, ss3637131137, ss3637913876, ss3640169003, ss3644567975, ss3651714721, ss3675621394, ss3738278355, ss3744086457, ss3744383981, ss3744762497, ss3749442103, ss3772262374, ss3786984825, ss3792121009, ss3797003337, ss3832685994, ss3876507030, ss3924901523, ss3984652526, ss3985539399, ss5202542420, ss5315553401, ss5400339574, ss5510402799, ss5624277600, ss5651461159, ss5799845700, ss5836823716, ss5847392716, ss5847638366, ss5942772320, ss5979362359 NC_000011.9:69596522:G:A NC_000011.10:69781754:G:A (self)
71306276, 383266543, 632169, 855217, 84436886, 105005729, 3910204913, ss2183304996, ss3027170239, ss3692019582, ss3725252618, ss3771633748, ss3814781307, ss4889460073, ss5287846399, ss5482968980, ss5583780341, ss5750599782, ss5812518073, ss5850023933, ss5920452679 NC_000011.10:69781754:G:A NC_000011.10:69781754:G:A (self)
ss16146054 NT_078088.2:455645:G:A NC_000011.10:69781754:G:A (self)
ss5481189, ss5691569, ss38681975, ss66431406, ss69319818, ss76204565, ss81992626, ss156442737, ss160660082, ss172803382, ss173685247 NT_167190.1:14902317:G:A NC_000011.10:69781754:G:A (self)
3910204913 NC_000011.10:69781754:G:C NC_000011.10:69781754:G:C (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 rs4084127

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.post774+babeb33