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dbSNP Short Genetic Variations

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.

rs3100865

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr1:2889542 (GRCh38.p13) 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
T=0.481458 (127437/264690, TOPMED)
G=0.315056 (77311/245388, ALFA)
T=0.33549 (26142/77922, PAGE_STUDY) (+ 16 more)
T=0.36038 (6040/16760, 8.3KJPN)
T=0.3782 (1894/5008, 1000G)
G=0.3362 (1506/4480, Estonian)
G=0.2927 (1128/3854, ALSPAC)
G=0.2913 (1080/3708, TWINSUK)
T=0.3801 (1113/2928, KOREAN)
T=0.4323 (900/2082, HGDP_Stanford)
T=0.3335 (629/1886, HapMap)
T=0.3832 (702/1832, Korea1K)
G=0.303 (182/600, NorthernSweden)
T=0.222 (98/442, SGDP_PRJ)
G=0.435 (94/216, Qatari)
T=0.346 (72/208, Vietnamese)
G=0.46 (24/52, Ancient Sardinia)
T=0.41 (18/44, Siberian)
G=0.30 (12/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
None
Publications
0 citations
Genomic View
See rs on genome
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.p13 chr 1 NC_000001.11:g.2889542T>A
GRCh38.p13 chr 1 NC_000001.11:g.2889542T>C
GRCh38.p13 chr 1 NC_000001.11:g.2889542T>G
GRCh37.p13 chr 1 NC_000001.10:g.2806107T>A
GRCh37.p13 chr 1 NC_000001.10:g.2806107T>C
GRCh37.p13 chr 1 NC_000001.10:g.2806107T>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

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: 20201027095038
Population Group Sample Size Ref Allele Alt Allele
Total Global 245388 T=0.684944 A=0.000000, G=0.315056
European Sub 214814 T=0.711457 A=0.000000, G=0.288543
African Sub 4242 T=0.1714 A=0.0000, G=0.8286
African Others Sub 154 T=0.013 A=0.000, G=0.987
African American Sub 4088 T=0.1773 A=0.0000, G=0.8227
Asian Sub 3460 T=0.4078 A=0.0000, G=0.5922
East Asian Sub 2204 T=0.4093 A=0.0000, G=0.5907
Other Asian Sub 1256 T=0.4053 A=0.0000, G=0.5947
Latin American 1 Sub 580 T=0.572 A=0.000, G=0.428
Latin American 2 Sub 5086 T=0.4725 A=0.0000, G=0.5275
South Asian Sub 4956 T=0.5454 A=0.0000, G=0.4546
Other Sub 12250 T=0.62612 A=0.00000, G=0.37388


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=0.481458 G=0.518542
The PAGE Study Global Study-wide 77922 T=0.33549 G=0.66451
The PAGE Study AfricanAmerican Sub 32112 T=0.16551 G=0.83449
The PAGE Study Mexican Sub 10732 T=0.45760 G=0.54240
The PAGE Study Asian Sub 8238 T=0.3753 G=0.6247
The PAGE Study PuertoRican Sub 7870 T=0.5084 G=0.4916
The PAGE Study NativeHawaiian Sub 4494 T=0.4729 G=0.5271
The PAGE Study Cuban Sub 4184 T=0.5664 G=0.4336
The PAGE Study Dominican Sub 3794 T=0.3946 G=0.6054
The PAGE Study CentralAmerican Sub 2428 T=0.3847 G=0.6153
The PAGE Study SouthAmerican Sub 1964 T=0.4104 G=0.5896
The PAGE Study NativeAmerican Sub 1256 T=0.5358 G=0.4642
The PAGE Study SouthAsian Sub 850 T=0.492 G=0.508
8.3KJPN JAPANESE Study-wide 16760 T=0.36038 G=0.63962
1000Genomes Global Study-wide 5008 T=0.3782 G=0.6218
1000Genomes African Sub 1322 T=0.0446 G=0.9554
1000Genomes East Asian Sub 1008 T=0.3333 G=0.6667
1000Genomes Europe Sub 1006 T=0.6690 G=0.3310
1000Genomes South Asian Sub 978 T=0.489 G=0.511
1000Genomes American Sub 694 T=0.501 G=0.499
Genetic variation in the Estonian population Estonian Study-wide 4480 T=0.6638 G=0.3362
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 T=0.7073 G=0.2927
UK 10K study - Twins TWIN COHORT Study-wide 3708 T=0.7087 G=0.2913
KOREAN population from KRGDB KOREAN Study-wide 2928 T=0.3801 C=0.0000, G=0.6199
HGDP-CEPH-db Supplement 1 Global Study-wide 2082 T=0.4323 G=0.5677
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 T=0.321 G=0.679
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 T=0.587 G=0.413
HGDP-CEPH-db Supplement 1 Middle_Est Sub 348 T=0.624 G=0.376
HGDP-CEPH-db Supplement 1 Europe Sub 320 T=0.700 G=0.300
HGDP-CEPH-db Supplement 1 Africa Sub 242 T=0.029 G=0.971
HGDP-CEPH-db Supplement 1 America Sub 216 T=0.241 G=0.759
HGDP-CEPH-db Supplement 1 Oceania Sub 72 T=0.08 G=0.92
HapMap Global Study-wide 1886 T=0.3335 G=0.6665
HapMap American Sub 770 T=0.497 G=0.503
HapMap African Sub 688 T=0.055 G=0.945
HapMap Asian Sub 252 T=0.349 G=0.651
HapMap Europe Sub 176 T=0.682 G=0.318
Korean Genome Project KOREAN Study-wide 1832 T=0.3832 G=0.6168
Northern Sweden ACPOP Study-wide 600 T=0.697 G=0.303
SGDP_PRJ Global Study-wide 442 T=0.222 G=0.778
Qatari Global Study-wide 216 T=0.565 G=0.435
A Vietnamese Genetic Variation Database Global Study-wide 208 T=0.346 G=0.654
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 52 T=0.54 G=0.46
Siberian Global Study-wide 44 T=0.41 G=0.59
The Danish reference pan genome Danish Study-wide 40 T=0.70 G=0.30
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.p13 chr 1 NC_000001.11:g.2889542= NC_000001.11:g.2889542T>A NC_000001.11:g.2889542T>C NC_000001.11:g.2889542T>G
GRCh37.p13 chr 1 NC_000001.10:g.2806107= NC_000001.10:g.2806107T>A NC_000001.10:g.2806107T>C NC_000001.10:g.2806107T>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#.

122 SubSNP, 21 Frequency submissions
No Submitter Submission ID Date (Build)
1 SC_JCM ss4338757 Mar 26, 2002 (103)
2 SC_SNP ss12992588 Dec 05, 2003 (119)
3 CSHL-HAPMAP ss16416864 Feb 27, 2004 (120)
4 CSHL-HAPMAP ss17346809 Feb 27, 2004 (120)
5 ABI ss41193138 Mar 15, 2006 (126)
6 ILLUMINA ss66778402 Dec 01, 2006 (127)
7 ILLUMINA ss67289934 Dec 01, 2006 (127)
8 ILLUMINA ss67693354 Dec 01, 2006 (127)
9 ILLUMINA ss70768509 May 23, 2008 (130)
10 ILLUMINA ss71343473 May 17, 2007 (127)
11 ILLUMINA ss75788341 Dec 07, 2007 (129)
12 ILLUMINA ss79158122 Dec 14, 2007 (130)
13 HGSV ss83465690 Dec 14, 2007 (130)
14 KRIBB_YJKIM ss84147181 Dec 14, 2007 (130)
15 BCMHGSC_JDW ss87169549 Mar 23, 2008 (129)
16 BGI ss105113950 Dec 01, 2009 (131)
17 1000GENOMES ss109955418 Jan 24, 2009 (130)
18 ILLUMINA-UK ss118446512 Feb 14, 2009 (130)
19 ILLUMINA ss122168879 Dec 01, 2009 (131)
20 ENSEMBL ss137760643 Dec 01, 2009 (131)
21 ILLUMINA ss154253568 Dec 01, 2009 (131)
22 GMI ss154548561 Dec 01, 2009 (131)
23 ILLUMINA ss159430368 Dec 01, 2009 (131)
24 ILLUMINA ss160610247 Dec 01, 2009 (131)
25 ENSEMBL ss161243066 Dec 01, 2009 (131)
26 ILLUMINA ss171536374 Jul 04, 2010 (132)
27 ILLUMINA ss173561103 Jul 04, 2010 (132)
28 BUSHMAN ss197910869 Jul 04, 2010 (132)
29 1000GENOMES ss218197865 Jul 14, 2010 (132)
30 1000GENOMES ss230400677 Jul 14, 2010 (132)
31 1000GENOMES ss238119831 Jul 15, 2010 (132)
32 GMI ss275688310 May 04, 2012 (137)
33 PJP ss290496854 May 09, 2011 (134)
34 ILLUMINA ss480751380 May 04, 2012 (137)
35 ILLUMINA ss480767290 May 04, 2012 (137)
36 ILLUMINA ss481655425 Sep 08, 2015 (146)
37 ILLUMINA ss485170465 May 04, 2012 (137)
38 EXOME_CHIP ss491284814 May 04, 2012 (137)
39 TISHKOFF ss553726296 Apr 25, 2013 (138)
40 SSMP ss647529986 Apr 25, 2013 (138)
41 ILLUMINA ss780799967 Sep 08, 2015 (146)
42 ILLUMINA ss783031435 Sep 08, 2015 (146)
43 ILLUMINA ss783481330 Sep 08, 2015 (146)
44 ILLUMINA ss825488640 Apr 01, 2015 (144)
45 ILLUMINA ss832289063 Sep 08, 2015 (146)
46 ILLUMINA ss832941976 Jul 12, 2019 (153)
47 EVA-GONL ss974786824 Aug 21, 2014 (142)
48 JMKIDD_LAB ss1067621489 Aug 21, 2014 (142)
49 1000GENOMES ss1289415875 Aug 21, 2014 (142)
50 DDI ss1425690225 Apr 01, 2015 (144)
51 EVA_GENOME_DK ss1573856955 Apr 01, 2015 (144)
52 EVA_DECODE ss1584146361 Apr 01, 2015 (144)
53 EVA_UK10K_ALSPAC ss1599409481 Apr 01, 2015 (144)
54 EVA_UK10K_TWINSUK ss1642403514 Apr 01, 2015 (144)
55 EVA_SVP ss1712306228 Apr 01, 2015 (144)
56 ILLUMINA ss1751913918 Sep 08, 2015 (146)
57 ILLUMINA ss1751913919 Sep 08, 2015 (146)
58 HAMMER_LAB ss1793755176 Sep 08, 2015 (146)
59 ILLUMINA ss1917721513 Feb 12, 2016 (147)
60 WEILL_CORNELL_DGM ss1917981648 Feb 12, 2016 (147)
61 ILLUMINA ss1945982490 Feb 12, 2016 (147)
62 ILLUMINA ss1945982491 Feb 12, 2016 (147)
63 ILLUMINA ss1958233410 Feb 12, 2016 (147)
64 ILLUMINA ss1958233411 Feb 12, 2016 (147)
65 JJLAB ss2019507112 Sep 14, 2016 (149)
66 USC_VALOUEV ss2147496950 Dec 20, 2016 (150)
67 HUMAN_LONGEVITY ss2159501605 Dec 20, 2016 (150)
68 TOPMED ss2321657352 Dec 20, 2016 (150)
69 SYSTEMSBIOZJU ss2624269383 Nov 08, 2017 (151)
70 ILLUMINA ss2632467341 Nov 08, 2017 (151)
71 ILLUMINA ss2632467342 Nov 08, 2017 (151)
72 ILLUMINA ss2634995443 Nov 08, 2017 (151)
73 GRF ss2697390519 Nov 08, 2017 (151)
74 ILLUMINA ss2710663865 Nov 08, 2017 (151)
75 GNOMAD ss2750877122 Nov 08, 2017 (151)
76 SWEGEN ss2986187265 Nov 08, 2017 (151)
77 ILLUMINA ss3021046334 Nov 08, 2017 (151)
78 ILLUMINA ss3021046335 Nov 08, 2017 (151)
79 BIOINF_KMB_FNS_UNIBA ss3023517334 Nov 08, 2017 (151)
80 TOPMED ss3066918661 Nov 08, 2017 (151)
81 CSHL ss3343284344 Nov 08, 2017 (151)
82 ILLUMINA ss3625523717 Oct 11, 2018 (152)
83 ILLUMINA ss3633571865 Oct 11, 2018 (152)
84 ILLUMINA ss3634302987 Oct 11, 2018 (152)
85 ILLUMINA ss3634302988 Oct 11, 2018 (152)
86 ILLUMINA ss3635266053 Oct 11, 2018 (152)
87 ILLUMINA ss3635979344 Oct 11, 2018 (152)
88 ILLUMINA ss3637016401 Oct 11, 2018 (152)
89 ILLUMINA ss3637733314 Oct 11, 2018 (152)
90 ILLUMINA ss3638888041 Oct 11, 2018 (152)
91 ILLUMINA ss3639440743 Oct 11, 2018 (152)
92 ILLUMINA ss3640010352 Oct 11, 2018 (152)
93 ILLUMINA ss3640010353 Oct 11, 2018 (152)
94 ILLUMINA ss3640973457 Oct 11, 2018 (152)
95 ILLUMINA ss3641267270 Oct 11, 2018 (152)
96 ILLUMINA ss3642747539 Oct 11, 2018 (152)
97 ILLUMINA ss3644478343 Oct 11, 2018 (152)
98 ILLUMINA ss3644478344 Oct 11, 2018 (152)
99 ILLUMINA ss3651368926 Oct 11, 2018 (152)
100 ILLUMINA ss3651368927 Oct 11, 2018 (152)
101 EGCUT_WGS ss3654288229 Jul 12, 2019 (153)
102 EVA_DECODE ss3686029779 Jul 12, 2019 (153)
103 ACPOP ss3726732018 Jul 12, 2019 (153)
104 ILLUMINA ss3744040927 Jul 12, 2019 (153)
105 ILLUMINA ss3744337949 Jul 12, 2019 (153)
106 ILLUMINA ss3744603913 Jul 12, 2019 (153)
107 ILLUMINA ss3744603914 Jul 12, 2019 (153)
108 EVA ss3745743366 Jul 12, 2019 (153)
109 PAGE_CC ss3770780010 Jul 12, 2019 (153)
110 ILLUMINA ss3772105642 Jul 12, 2019 (153)
111 ILLUMINA ss3772105643 Jul 12, 2019 (153)
112 KHV_HUMAN_GENOMES ss3798765857 Jul 12, 2019 (153)
113 EVA ss3825989519 Apr 25, 2020 (154)
114 EVA ss3836382068 Apr 25, 2020 (154)
115 EVA ss3841786180 Apr 25, 2020 (154)
116 HGDP ss3847322306 Apr 25, 2020 (154)
117 SGDP_PRJ ss3848048703 Apr 25, 2020 (154)
118 KRGDB ss3892908127 Apr 25, 2020 (154)
119 KOGIC ss3943672088 Apr 25, 2020 (154)
120 EVA ss3984774500 Apr 25, 2021 (155)
121 TOPMED ss4437033831 Apr 25, 2021 (155)
122 TOMMO_GENOMICS ss5142160738 Apr 25, 2021 (155)
123 1000Genomes NC_000001.10 - 2806107 Oct 11, 2018 (152)
124 The Avon Longitudinal Study of Parents and Children NC_000001.10 - 2806107 Oct 11, 2018 (152)
125 Genetic variation in the Estonian population NC_000001.10 - 2806107 Oct 11, 2018 (152)
126 The Danish reference pan genome NC_000001.10 - 2806107 Apr 25, 2020 (154)
127 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 631808 (NC_000001.11:2889541:T:A 2/139758)
Row 631809 (NC_000001.11:2889541:T:G 69820/139704)

- Apr 25, 2021 (155)
128 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 631808 (NC_000001.11:2889541:T:A 2/139758)
Row 631809 (NC_000001.11:2889541:T:G 69820/139704)

- Apr 25, 2021 (155)
129 HGDP-CEPH-db Supplement 1 NC_000001.9 - 2795967 Apr 25, 2020 (154)
130 HapMap NC_000001.11 - 2889542 Apr 25, 2020 (154)
131 KOREAN population from KRGDB NC_000001.10 - 2806107 Apr 25, 2020 (154)
132 Korean Genome Project NC_000001.11 - 2889542 Apr 25, 2020 (154)
133 Northern Sweden NC_000001.10 - 2806107 Jul 12, 2019 (153)
134 The PAGE Study NC_000001.11 - 2889542 Jul 12, 2019 (153)
135 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000001.10 - 2806107 Apr 25, 2021 (155)
136 Qatari NC_000001.10 - 2806107 Apr 25, 2020 (154)
137 SGDP_PRJ NC_000001.10 - 2806107 Apr 25, 2020 (154)
138 Siberian NC_000001.10 - 2806107 Apr 25, 2020 (154)
139 8.3KJPN NC_000001.10 - 2806107 Apr 25, 2021 (155)
140 TopMed NC_000001.11 - 2889542 Apr 25, 2021 (155)
141 UK 10K study - Twins NC_000001.10 - 2806107 Oct 11, 2018 (152)
142 A Vietnamese Genetic Variation Database NC_000001.10 - 2806107 Jul 12, 2019 (153)
143 ALFA NC_000001.11 - 2889542 Apr 25, 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)
rs57014980 May 23, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss2750877122 NC_000001.10:2806106:T:A NC_000001.11:2889541:T:A (self)
15196221964 NC_000001.11:2889541:T:A NC_000001.11:2889541:T:A
85521, ss3892908127 NC_000001.10:2806106:T:C NC_000001.11:2889541:T:C (self)
ss83465690, ss3638888041, ss3639440743 NC_000001.8:2829263:T:G NC_000001.11:2889541:T:G (self)
198, ss87169549, ss109955418, ss118446512, ss197910869, ss275688310, ss290496854, ss480751380, ss825488640, ss1584146361, ss1712306228, ss2634995443, ss3642747539, ss3847322306 NC_000001.9:2795966:T:G NC_000001.11:2889541:T:G (self)
82875, 34360, 26477, 1364189, 85521, 16883, 427, 23578, 65683, 13304, 130045, 34360, 7005, ss218197865, ss230400677, ss238119831, ss480767290, ss481655425, ss485170465, ss491284814, ss553726296, ss647529986, ss780799967, ss783031435, ss783481330, ss832289063, ss832941976, ss974786824, ss1067621489, ss1289415875, ss1425690225, ss1573856955, ss1599409481, ss1642403514, ss1751913918, ss1751913919, ss1793755176, ss1917721513, ss1917981648, ss1945982490, ss1945982491, ss1958233410, ss1958233411, ss2019507112, ss2147496950, ss2321657352, ss2624269383, ss2632467341, ss2632467342, ss2697390519, ss2710663865, ss2750877122, ss2986187265, ss3021046334, ss3021046335, ss3343284344, ss3625523717, ss3633571865, ss3634302987, ss3634302988, ss3635266053, ss3635979344, ss3637016401, ss3637733314, ss3640010352, ss3640010353, ss3640973457, ss3641267270, ss3644478343, ss3644478344, ss3651368926, ss3651368927, ss3654288229, ss3726732018, ss3744040927, ss3744337949, ss3744603913, ss3744603914, ss3745743366, ss3772105642, ss3772105643, ss3825989519, ss3836382068, ss3848048703, ss3892908127, ss3984774500, ss5142160738 NC_000001.10:2806106:T:G NC_000001.11:2889541:T:G (self)
1520, 50089, 1479, 394319, 640166, 15196221964, ss2159501605, ss3023517334, ss3066918661, ss3686029779, ss3770780010, ss3798765857, ss3841786180, ss3943672088, ss4437033831 NC_000001.11:2889541:T:G NC_000001.11:2889541:T:G (self)
ss12992588, ss16416864, ss17346809 NT_004321.15:112881:T:G NC_000001.11:2889541:T:G (self)
ss4338757, ss41193138, ss66778402, ss67289934, ss67693354, ss70768509, ss71343473, ss75788341, ss79158122, ss84147181, ss105113950, ss122168879, ss137760643, ss154253568, ss154548561, ss159430368, ss160610247, ss161243066, ss171536374, ss173561103 NT_004350.19:2284738:T:G NC_000001.11:2889541: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 rs3100865

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.post596+ae089ad