Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

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.

rs3806650

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr3:165838023 (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 / G>T
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.344478 (91180/264690, TOPMED)
G=0.286636 (40958/142892, ALFA)
G=0.341090 (47711/139878, GnomAD) (+ 19 more)
G=0.35682 (28074/78678, PAGE_STUDY)
G=0.21912 (6192/28258, 14KJPN)
G=0.21647 (3628/16760, 8.3KJPN)
G=0.3318 (2125/6404, 1000G_30x)
G=0.3257 (1631/5008, 1000G)
G=0.2408 (1079/4480, Estonian)
G=0.2717 (1047/3854, ALSPAC)
G=0.2783 (1032/3708, TWINSUK)
G=0.2464 (722/2930, KOREAN)
G=0.2331 (427/1832, Korea1K)
G=0.3873 (643/1660, HapMap)
G=0.236 (236/998, GoNL)
G=0.255 (202/792, PRJEB37584)
G=0.293 (176/600, NorthernSweden)
G=0.192 (95/494, SGDP_PRJ)
G=0.361 (78/216, Qatari)
G=0.157 (33/210, Vietnamese)
G=0.20 (11/54, Siberian)
G=0.30 (12/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
BCHE : 2KB Upstream 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 147924 G=0.288351 A=0.711649
European Sub 127322 G=0.278514 A=0.721486
African Sub 7410 G=0.5131 A=0.4869
African Others Sub 278 G=0.626 A=0.374
African American Sub 7132 G=0.5087 A=0.4913
Asian Sub 3406 G=0.2161 A=0.7839
East Asian Sub 2748 G=0.2373 A=0.7627
Other Asian Sub 658 G=0.128 A=0.872
Latin American 1 Sub 618 G=0.350 A=0.650
Latin American 2 Sub 3228 G=0.2150 A=0.7850
South Asian Sub 308 G=0.302 A=0.698
Other Sub 5632 G=0.2933 A=0.7067


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=0.344478 A=0.655522
Allele Frequency Aggregator Total Global 142892 G=0.286636 A=0.713364
Allele Frequency Aggregator European Sub 124228 G=0.278560 A=0.721440
Allele Frequency Aggregator African Sub 6272 G=0.5132 A=0.4868
Allele Frequency Aggregator Other Sub 4832 G=0.2887 A=0.7113
Allele Frequency Aggregator Asian Sub 3406 G=0.2161 A=0.7839
Allele Frequency Aggregator Latin American 2 Sub 3228 G=0.2150 A=0.7850
Allele Frequency Aggregator Latin American 1 Sub 618 G=0.350 A=0.650
Allele Frequency Aggregator South Asian Sub 308 G=0.302 A=0.698
gnomAD - Genomes Global Study-wide 139878 G=0.341090 A=0.658910
gnomAD - Genomes European Sub 75810 G=0.26940 A=0.73060
gnomAD - Genomes African Sub 41862 G=0.51749 A=0.48251
gnomAD - Genomes American Sub 13608 G=0.23854 A=0.76146
gnomAD - Genomes Ashkenazi Jewish Sub 3324 G=0.3243 A=0.6757
gnomAD - Genomes East Asian Sub 3124 G=0.2001 A=0.7999
gnomAD - Genomes Other Sub 2150 G=0.3144 A=0.6856
The PAGE Study Global Study-wide 78678 G=0.35682 A=0.64318
The PAGE Study AfricanAmerican Sub 32494 G=0.51320 A=0.48680
The PAGE Study Mexican Sub 10810 G=0.20768 A=0.79232
The PAGE Study Asian Sub 8316 G=0.2083 A=0.7917
The PAGE Study PuertoRican Sub 7918 G=0.2983 A=0.7017
The PAGE Study NativeHawaiian Sub 4534 G=0.1460 A=0.8540
The PAGE Study Cuban Sub 4230 G=0.3208 A=0.6792
The PAGE Study Dominican Sub 3828 G=0.4039 A=0.5961
The PAGE Study CentralAmerican Sub 2450 G=0.2131 A=0.7869
The PAGE Study SouthAmerican Sub 1982 G=0.1917 A=0.8083
The PAGE Study NativeAmerican Sub 1260 G=0.2706 A=0.7294
The PAGE Study SouthAsian Sub 856 G=0.293 A=0.707
14KJPN JAPANESE Study-wide 28258 G=0.21912 A=0.78088
8.3KJPN JAPANESE Study-wide 16760 G=0.21647 A=0.78353
1000Genomes_30x Global Study-wide 6404 G=0.3318 A=0.6682
1000Genomes_30x African Sub 1786 G=0.5622 A=0.4378
1000Genomes_30x Europe Sub 1266 G=0.2654 A=0.7346
1000Genomes_30x South Asian Sub 1202 G=0.2745 A=0.7255
1000Genomes_30x East Asian Sub 1170 G=0.2077 A=0.7923
1000Genomes_30x American Sub 980 G=0.216 A=0.784
1000Genomes Global Study-wide 5008 G=0.3257 A=0.6743
1000Genomes African Sub 1322 G=0.5598 A=0.4402
1000Genomes East Asian Sub 1008 G=0.2063 A=0.7937
1000Genomes Europe Sub 1006 G=0.2684 A=0.7316
1000Genomes South Asian Sub 978 G=0.269 A=0.731
1000Genomes American Sub 694 G=0.216 A=0.784
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.2408 A=0.7592
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.2717 A=0.7283
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.2783 A=0.7217
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.2464 A=0.7536, C=0.0000, T=0.0000
Korean Genome Project KOREAN Study-wide 1832 G=0.2331 A=0.7669
HapMap Global Study-wide 1660 G=0.3873 A=0.6127
HapMap African Sub 686 G=0.525 A=0.475
HapMap American Sub 544 G=0.300 A=0.700
HapMap Asian Sub 254 G=0.244 A=0.756
HapMap Europe Sub 176 G=0.330 A=0.670
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.236 A=0.764
CNV burdens in cranial meningiomas Global Study-wide 792 G=0.255 A=0.745
CNV burdens in cranial meningiomas CRM Sub 792 G=0.255 A=0.745
Northern Sweden ACPOP Study-wide 600 G=0.293 A=0.707
SGDP_PRJ Global Study-wide 494 G=0.192 A=0.808
Qatari Global Study-wide 216 G=0.361 A=0.639
A Vietnamese Genetic Variation Database Global Study-wide 210 G=0.157 A=0.843
Siberian Global Study-wide 54 G=0.20 A=0.80
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 3 NC_000003.12:g.165838023G>A
GRCh38.p14 chr 3 NC_000003.12:g.165838023G>C
GRCh38.p14 chr 3 NC_000003.12:g.165838023G>T
GRCh37.p13 chr 3 NC_000003.11:g.165555811G>A
GRCh37.p13 chr 3 NC_000003.11:g.165555811G>C
GRCh37.p13 chr 3 NC_000003.11:g.165555811G>T
BCHE RefSeqGene NG_009031.1:g.4443C>T
BCHE RefSeqGene NG_009031.1:g.4443C>G
BCHE RefSeqGene NG_009031.1:g.4443C>A
Gene: BCHE, butyrylcholinesterase (minus strand) : 2KB Upstream Variant
Molecule type Change Amino acid[Codon] SO Term
BCHE transcript variant 1 NM_000055.4:c. N/A Upstream Transcript Variant
BCHE transcript variant 2 NR_137635.2:n. N/A Upstream Transcript Variant
BCHE transcript variant 3 NR_137636.2:n. N/A Upstream 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 G= A C T
GRCh38.p14 chr 3 NC_000003.12:g.165838023= NC_000003.12:g.165838023G>A NC_000003.12:g.165838023G>C NC_000003.12:g.165838023G>T
GRCh37.p13 chr 3 NC_000003.11:g.165555811= NC_000003.11:g.165555811G>A NC_000003.11:g.165555811G>C NC_000003.11:g.165555811G>T
BCHE RefSeqGene NG_009031.1:g.4443= NG_009031.1:g.4443C>T NG_009031.1:g.4443C>G NG_009031.1:g.4443C>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#.

119 SubSNP, 22 Frequency submissions
No Submitter Submission ID Date (Build)
1 YUSUKE ss4993043 Aug 28, 2002 (107)
2 BCM_SSAHASNP ss14168599 Dec 05, 2003 (119)
3 SC_SNP ss15749821 Feb 27, 2004 (120)
4 CSHL-HAPMAP ss19507788 Feb 27, 2004 (120)
5 CSHL-HAPMAP ss20149072 Feb 27, 2004 (120)
6 SSAHASNP ss21890545 Apr 05, 2004 (121)
7 PERLEGEN ss23356054 Sep 20, 2004 (123)
8 ABI ss44378978 Mar 13, 2006 (126)
9 AFFY ss66353232 Nov 29, 2006 (127)
10 ILLUMINA ss75154344 Dec 06, 2007 (129)
11 AFFY ss76066700 Dec 08, 2007 (130)
12 HGSV ss80828907 Dec 16, 2007 (130)
13 KRIBB_YJKIM ss81963042 Dec 15, 2007 (130)
14 HGSV ss85725185 Dec 16, 2007 (130)
15 BCMHGSC_JDW ss92361333 Mar 24, 2008 (129)
16 HUMANGENOME_JCVI ss99148060 Feb 06, 2009 (130)
17 BGI ss104008193 Dec 01, 2009 (131)
18 1000GENOMES ss111294575 Jan 25, 2009 (130)
19 1000GENOMES ss112663570 Jan 25, 2009 (130)
20 ILLUMINA-UK ss117363964 Feb 14, 2009 (130)
21 ENSEMBL ss135437528 Dec 01, 2009 (131)
22 ENSEMBL ss139277606 Dec 01, 2009 (131)
23 GMI ss156469231 Dec 01, 2009 (131)
24 COMPLETE_GENOMICS ss162799904 Jul 04, 2010 (132)
25 COMPLETE_GENOMICS ss164880206 Jul 04, 2010 (132)
26 COMPLETE_GENOMICS ss167408985 Jul 04, 2010 (132)
27 AFFY ss172383002 Jun 24, 2010 (142)
28 ILLUMINA ss173647417 Jul 04, 2010 (132)
29 BUSHMAN ss203479569 Jul 04, 2010 (132)
30 BCM-HGSC-SUB ss206047600 Jul 04, 2010 (132)
31 1000GENOMES ss220557246 Jul 14, 2010 (132)
32 1000GENOMES ss232127442 Jul 14, 2010 (132)
33 1000GENOMES ss239478433 Jul 15, 2010 (132)
34 ILLUMINA ss244297518 Jul 04, 2010 (132)
35 GMI ss277441826 May 04, 2012 (137)
36 PJP ss292967640 May 09, 2011 (134)
37 ILLUMINA ss483582373 May 04, 2012 (137)
38 ILLUMINA ss484502840 May 04, 2012 (137)
39 ILLUMINA ss535788002 Sep 08, 2015 (146)
40 TISHKOFF ss557091780 Apr 25, 2013 (138)
41 SSMP ss650834448 Apr 25, 2013 (138)
42 ILLUMINA ss780331701 Sep 08, 2015 (146)
43 ILLUMINA ss782234621 Sep 08, 2015 (146)
44 ILLUMINA ss835819033 Sep 08, 2015 (146)
45 EVA-GONL ss979412670 Aug 21, 2014 (142)
46 JMKIDD_LAB ss1071022124 Aug 21, 2014 (142)
47 1000GENOMES ss1307114211 Aug 21, 2014 (142)
48 DDI ss1429661286 Apr 01, 2015 (144)
49 EVA_GENOME_DK ss1580280738 Apr 01, 2015 (144)
50 EVA_DECODE ss1588906443 Apr 01, 2015 (144)
51 EVA_UK10K_ALSPAC ss1608719670 Apr 01, 2015 (144)
52 EVA_UK10K_TWINSUK ss1651713703 Apr 01, 2015 (144)
53 EVA_SVP ss1712628986 Apr 01, 2015 (144)
54 HAMMER_LAB ss1800378656 Sep 08, 2015 (146)
55 WEILL_CORNELL_DGM ss1922635312 Feb 12, 2016 (147)
56 ILLUMINA ss1946101488 Feb 12, 2016 (147)
57 ILLUMINA ss1958625765 Feb 12, 2016 (147)
58 GENOMED ss1969580571 Jul 19, 2016 (147)
59 JJLAB ss2021892451 Sep 14, 2016 (149)
60 ILLUMINA ss2095140014 Dec 20, 2016 (150)
61 USC_VALOUEV ss2149988525 Dec 20, 2016 (150)
62 HUMAN_LONGEVITY ss2257825560 Dec 20, 2016 (150)
63 SYSTEMSBIOZJU ss2625447364 Nov 08, 2017 (151)
64 ILLUMINA ss2634039256 Nov 08, 2017 (151)
65 GRF ss2705408329 Nov 08, 2017 (151)
66 ILLUMINA ss2710990773 Nov 08, 2017 (151)
67 GNOMAD ss2801873685 Nov 08, 2017 (151)
68 SWEGEN ss2993579039 Nov 08, 2017 (151)
69 ILLUMINA ss3022310122 Nov 08, 2017 (151)
70 BIOINF_KMB_FNS_UNIBA ss3024714920 Nov 08, 2017 (151)
71 CSHL ss3345377329 Nov 08, 2017 (151)
72 ILLUMINA ss3625830734 Oct 12, 2018 (152)
73 ILLUMINA ss3628826972 Oct 12, 2018 (152)
74 ILLUMINA ss3631980690 Oct 12, 2018 (152)
75 ILLUMINA ss3638454354 Oct 12, 2018 (152)
76 ILLUMINA ss3642294856 Oct 12, 2018 (152)
77 ILLUMINA ss3643408198 Oct 12, 2018 (152)
78 ILLUMINA ss3644834147 Oct 12, 2018 (152)
79 URBANLAB ss3647578647 Oct 12, 2018 (152)
80 ILLUMINA ss3652790894 Oct 12, 2018 (152)
81 ILLUMINA ss3652790895 Oct 12, 2018 (152)
82 EGCUT_WGS ss3661522886 Jul 13, 2019 (153)
83 EVA_DECODE ss3710750035 Jul 13, 2019 (153)
84 ILLUMINA ss3726078376 Jul 13, 2019 (153)
85 ACPOP ss3730558710 Jul 13, 2019 (153)
86 ILLUMINA ss3744225643 Jul 13, 2019 (153)
87 EVA ss3760987465 Jul 13, 2019 (153)
88 PAGE_CC ss3771080669 Jul 13, 2019 (153)
89 PACBIO ss3784528256 Jul 13, 2019 (153)
90 PACBIO ss3790011935 Jul 13, 2019 (153)
91 PACBIO ss3794886580 Jul 13, 2019 (153)
92 KHV_HUMAN_GENOMES ss3804122288 Jul 13, 2019 (153)
93 EVA ss3828197160 Apr 25, 2020 (154)
94 EVA ss3837532353 Apr 25, 2020 (154)
95 EVA ss3842964252 Apr 25, 2020 (154)
96 SGDP_PRJ ss3857475171 Apr 25, 2020 (154)
97 KRGDB ss3903538136 Apr 25, 2020 (154)
98 KOGIC ss3952869640 Apr 25, 2020 (154)
99 EVA ss3984518609 Apr 26, 2021 (155)
100 EVA ss4017117287 Apr 26, 2021 (155)
101 TOPMED ss4591987298 Apr 26, 2021 (155)
102 TOMMO_GENOMICS ss5162662211 Apr 26, 2021 (155)
103 1000G_HIGH_COVERAGE ss5256860497 Oct 12, 2022 (156)
104 EVA ss5314909435 Oct 12, 2022 (156)
105 EVA ss5344793083 Oct 12, 2022 (156)
106 HUGCELL_USP ss5455918174 Oct 12, 2022 (156)
107 EVA ss5507296393 Oct 12, 2022 (156)
108 1000G_HIGH_COVERAGE ss5536746057 Oct 12, 2022 (156)
109 SANFORD_IMAGENETICS ss5624537305 Oct 12, 2022 (156)
110 SANFORD_IMAGENETICS ss5633667726 Oct 12, 2022 (156)
111 TOMMO_GENOMICS ss5695849530 Oct 12, 2022 (156)
112 YY_MCH ss5804456857 Oct 12, 2022 (156)
113 EVA ss5826802303 Oct 12, 2022 (156)
114 EVA ss5847230208 Oct 12, 2022 (156)
115 EVA ss5847989321 Oct 12, 2022 (156)
116 EVA ss5853942162 Oct 12, 2022 (156)
117 EVA ss5871962133 Oct 12, 2022 (156)
118 EVA ss5962039325 Oct 12, 2022 (156)
119 EVA ss5979678785 Oct 12, 2022 (156)
120 1000Genomes NC_000003.11 - 165555811 Oct 12, 2018 (152)
121 1000Genomes_30x NC_000003.12 - 165838023 Oct 12, 2022 (156)
122 The Avon Longitudinal Study of Parents and Children NC_000003.11 - 165555811 Oct 12, 2018 (152)
123 Genetic variation in the Estonian population NC_000003.11 - 165555811 Oct 12, 2018 (152)
124 The Danish reference pan genome NC_000003.11 - 165555811 Apr 25, 2020 (154)
125 gnomAD - Genomes NC_000003.12 - 165838023 Apr 26, 2021 (155)
126 Genome of the Netherlands Release 5 NC_000003.11 - 165555811 Apr 25, 2020 (154)
127 HapMap NC_000003.12 - 165838023 Apr 25, 2020 (154)
128 KOREAN population from KRGDB NC_000003.11 - 165555811 Apr 25, 2020 (154)
129 Korean Genome Project NC_000003.12 - 165838023 Apr 25, 2020 (154)
130 Northern Sweden NC_000003.11 - 165555811 Jul 13, 2019 (153)
131 The PAGE Study NC_000003.12 - 165838023 Jul 13, 2019 (153)
132 CNV burdens in cranial meningiomas NC_000003.11 - 165555811 Apr 26, 2021 (155)
133 Qatari NC_000003.11 - 165555811 Apr 25, 2020 (154)
134 SGDP_PRJ NC_000003.11 - 165555811 Apr 25, 2020 (154)
135 Siberian NC_000003.11 - 165555811 Apr 25, 2020 (154)
136 8.3KJPN NC_000003.11 - 165555811 Apr 26, 2021 (155)
137 14KJPN NC_000003.12 - 165838023 Oct 12, 2022 (156)
138 TopMed NC_000003.12 - 165838023 Apr 26, 2021 (155)
139 UK 10K study - Twins NC_000003.11 - 165555811 Oct 12, 2018 (152)
140 A Vietnamese Genetic Variation Database NC_000003.11 - 165555811 Jul 13, 2019 (153)
141 ALFA NC_000003.12 - 165838023 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)
rs56573658 May 26, 2008 (130)
rs60447440 Feb 27, 2009 (130)
rs61162023 May 26, 2008 (130)
rs111176015 Aug 21, 2014 (142)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss80828907, ss85725185 NC_000003.9:167038512:G:A NC_000003.12:165838022:G:A (self)
ss66353232, ss76066700, ss92361333, ss111294575, ss112663570, ss117363964, ss162799904, ss164880206, ss167408985, ss172383002, ss203479569, ss206047600, ss277441826, ss292967640, ss484502840, ss1588906443, ss1712628986, ss3643408198 NC_000003.10:167038504:G:A NC_000003.12:165838022:G:A (self)
18413990, 10258332, 7261134, 6445677, 4508110, 10715530, 3843575, 67962, 4677242, 9492151, 2504879, 20631518, 10258332, 2243541, ss220557246, ss232127442, ss239478433, ss483582373, ss535788002, ss557091780, ss650834448, ss780331701, ss782234621, ss835819033, ss979412670, ss1071022124, ss1307114211, ss1429661286, ss1580280738, ss1608719670, ss1651713703, ss1800378656, ss1922635312, ss1946101488, ss1958625765, ss1969580571, ss2021892451, ss2095140014, ss2149988525, ss2625447364, ss2634039256, ss2705408329, ss2710990773, ss2801873685, ss2993579039, ss3022310122, ss3345377329, ss3625830734, ss3628826972, ss3631980690, ss3638454354, ss3642294856, ss3644834147, ss3652790894, ss3652790895, ss3661522886, ss3730558710, ss3744225643, ss3760987465, ss3784528256, ss3790011935, ss3794886580, ss3828197160, ss3837532353, ss3857475171, ss3903538136, ss3984518609, ss4017117287, ss5162662211, ss5314909435, ss5344793083, ss5507296393, ss5624537305, ss5633667726, ss5826802303, ss5847230208, ss5847989321, ss5962039325, ss5979678785 NC_000003.11:165555810:G:A NC_000003.12:165838022:G:A (self)
24271992, 130808617, 2502613, 9247641, 302138, 29686634, 429364853, 10882340551, ss2257825560, ss3024714920, ss3647578647, ss3710750035, ss3726078376, ss3771080669, ss3804122288, ss3842964252, ss3952869640, ss4591987298, ss5256860497, ss5455918174, ss5536746057, ss5695849530, ss5804456857, ss5853942162, ss5871962133 NC_000003.12:165838022:G:A NC_000003.12:165838022:G:A (self)
ss14168599, ss15749821, ss19507788, ss20149072, ss21890545 NT_005612.14:72050968:G:A NC_000003.12:165838022:G:A (self)
ss4993043, ss23356054, ss44378978, ss75154344, ss81963042, ss99148060, ss104008193, ss135437528, ss139277606, ss156469231, ss173647417, ss244297518 NT_005612.16:72050956:G:A NC_000003.12:165838022:G:A (self)
10715530, ss3903538136 NC_000003.11:165555810:G:C NC_000003.12:165838022:G:C (self)
10715530, ss3903538136 NC_000003.11:165555810:G:T NC_000003.12:165838022:G:T (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 rs3806650

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