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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.

rs6671356

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr1:1104646 (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>C
Variation Type
SNV Single Nucleotide Variation
Frequency
C=0.256311 (67843/264690, TOPMED)
C=0.164047 (41599/253580, ALFA)
C=0.242986 (34020/140008, GnomAD) (+ 20 more)
C=0.31904 (25059/78544, PAGE_STUDY)
C=0.20373 (5757/28258, 14KJPN)
C=0.20656 (3462/16760, 8.3KJPN)
C=0.2873 (1840/6404, 1000G_30x)
C=0.2829 (1417/5008, 1000G)
C=0.1306 (585/4480, Estonian)
C=0.1256 (484/3854, ALSPAC)
C=0.1400 (519/3708, TWINSUK)
C=0.2283 (669/2930, KOREAN)
C=0.3095 (585/1890, HapMap)
C=0.2298 (421/1832, Korea1K)
C=0.1812 (204/1126, Daghestan)
C=0.124 (124/998, GoNL)
C=0.185 (141/762, PRJEB37584)
C=0.130 (78/600, NorthernSweden)
T=0.417 (91/218, SGDP_PRJ)
C=0.343 (74/216, Qatari)
C=0.134 (29/216, Vietnamese)
C=0.15 (6/40, GENOME_DK)
T=0.33 (6/18, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
C1orf159 : 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 258614 T=0.834727 C=0.165273
European Sub 226244 T=0.853052 C=0.146948
African Sub 11284 T=0.54085 C=0.45915
African Others Sub 434 T=0.493 C=0.507
African American Sub 10850 T=0.54276 C=0.45724
Asian Sub 3854 T=0.7878 C=0.2122
East Asian Sub 3122 T=0.7876 C=0.2124
Other Asian Sub 732 T=0.788 C=0.212
Latin American 1 Sub 1038 T=0.7505 C=0.2495
Latin American 2 Sub 6580 T=0.8125 C=0.1875
South Asian Sub 368 T=0.799 C=0.201
Other Sub 9246 T=0.7913 C=0.2087


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=0.743689 C=0.256311
Allele Frequency Aggregator Total Global 253580 T=0.835953 C=0.164047
Allele Frequency Aggregator European Sub 223150 T=0.853027 C=0.146973
Allele Frequency Aggregator African Sub 10144 T=0.53914 C=0.46086
Allele Frequency Aggregator Other Sub 8446 T=0.7937 C=0.2063
Allele Frequency Aggregator Latin American 2 Sub 6580 T=0.8125 C=0.1875
Allele Frequency Aggregator Asian Sub 3854 T=0.7878 C=0.2122
Allele Frequency Aggregator Latin American 1 Sub 1038 T=0.7505 C=0.2495
Allele Frequency Aggregator South Asian Sub 368 T=0.799 C=0.201
gnomAD - Genomes Global Study-wide 140008 T=0.757014 C=0.242986
gnomAD - Genomes European Sub 75872 T=0.86440 C=0.13560
gnomAD - Genomes African Sub 41888 T=0.54066 C=0.45934
gnomAD - Genomes American Sub 13648 T=0.80840 C=0.19160
gnomAD - Genomes Ashkenazi Jewish Sub 3318 T=0.7960 C=0.2040
gnomAD - Genomes East Asian Sub 3132 T=0.7883 C=0.2117
gnomAD - Genomes Other Sub 2150 T=0.7507 C=0.2493
The PAGE Study Global Study-wide 78544 T=0.68096 C=0.31904
The PAGE Study AfricanAmerican Sub 32442 T=0.54556 C=0.45444
The PAGE Study Mexican Sub 10790 T=0.78619 C=0.21381
The PAGE Study Asian Sub 8310 T=0.7959 C=0.2041
The PAGE Study PuertoRican Sub 7908 T=0.7605 C=0.2395
The PAGE Study NativeHawaiian Sub 4516 T=0.7708 C=0.2292
The PAGE Study Cuban Sub 4218 T=0.7914 C=0.2086
The PAGE Study Dominican Sub 3822 T=0.6941 C=0.3059
The PAGE Study CentralAmerican Sub 2448 T=0.7761 C=0.2239
The PAGE Study SouthAmerican Sub 1980 T=0.8348 C=0.1652
The PAGE Study NativeAmerican Sub 1258 T=0.7838 C=0.2162
The PAGE Study SouthAsian Sub 852 T=0.779 C=0.221
14KJPN JAPANESE Study-wide 28258 T=0.79627 C=0.20373
8.3KJPN JAPANESE Study-wide 16760 T=0.79344 C=0.20656
1000Genomes_30x Global Study-wide 6404 T=0.7127 C=0.2873
1000Genomes_30x African Sub 1786 T=0.4597 C=0.5403
1000Genomes_30x Europe Sub 1266 T=0.8720 C=0.1280
1000Genomes_30x South Asian Sub 1202 T=0.7604 C=0.2396
1000Genomes_30x East Asian Sub 1170 T=0.7795 C=0.2205
1000Genomes_30x American Sub 980 T=0.830 C=0.170
1000Genomes Global Study-wide 5008 T=0.7171 C=0.2829
1000Genomes African Sub 1322 T=0.4644 C=0.5356
1000Genomes East Asian Sub 1008 T=0.7778 C=0.2222
1000Genomes Europe Sub 1006 T=0.8658 C=0.1342
1000Genomes South Asian Sub 978 T=0.764 C=0.236
1000Genomes American Sub 694 T=0.829 C=0.171
Genetic variation in the Estonian population Estonian Study-wide 4480 T=0.8694 C=0.1306
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 T=0.8744 C=0.1256
UK 10K study - Twins TWIN COHORT Study-wide 3708 T=0.8600 C=0.1400
KOREAN population from KRGDB KOREAN Study-wide 2930 T=0.7717 C=0.2283
HapMap Global Study-wide 1890 T=0.6905 C=0.3095
HapMap American Sub 770 T=0.804 C=0.196
HapMap African Sub 690 T=0.512 C=0.488
HapMap Asian Sub 254 T=0.728 C=0.272
HapMap Europe Sub 176 T=0.841 C=0.159
Korean Genome Project KOREAN Study-wide 1832 T=0.7702 C=0.2298
Genome-wide autozygosity in Daghestan Global Study-wide 1126 T=0.8188 C=0.1812
Genome-wide autozygosity in Daghestan Daghestan Sub 622 T=0.844 C=0.156
Genome-wide autozygosity in Daghestan Near_East Sub 144 T=0.771 C=0.229
Genome-wide autozygosity in Daghestan Central Asia Sub 120 T=0.825 C=0.175
Genome-wide autozygosity in Daghestan Europe Sub 106 T=0.840 C=0.160
Genome-wide autozygosity in Daghestan South Asian Sub 98 T=0.70 C=0.30
Genome-wide autozygosity in Daghestan Caucasus Sub 36 T=0.81 C=0.19
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 T=0.876 C=0.124
CNV burdens in cranial meningiomas Global Study-wide 762 T=0.815 C=0.185
CNV burdens in cranial meningiomas CRM Sub 762 T=0.815 C=0.185
Northern Sweden ACPOP Study-wide 600 T=0.870 C=0.130
SGDP_PRJ Global Study-wide 218 T=0.417 C=0.583
Qatari Global Study-wide 216 T=0.657 C=0.343
A Vietnamese Genetic Variation Database Global Study-wide 216 T=0.866 C=0.134
The Danish reference pan genome Danish Study-wide 40 T=0.85 C=0.15
Siberian Global Study-wide 18 T=0.33 C=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 1 NC_000001.11:g.1104646T>C
GRCh37.p13 chr 1 NC_000001.10:g.1040026T>C
Gene: C1orf159, chromosome 1 open reading frame 159 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
C1orf159 transcript variant 1 NM_001330306.2:c.-136+103…

NM_001330306.2:c.-136+10376A>G

N/A Intron Variant
C1orf159 transcript variant 3 NM_001363525.2:c.-136+103…

NM_001363525.2:c.-136+10376A>G

N/A Intron Variant
C1orf159 transcript variant 2 NM_017891.5:c.-136+11414A…

NM_017891.5:c.-136+11414A>G

N/A Intron 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= C
GRCh38.p14 chr 1 NC_000001.11:g.1104646= NC_000001.11:g.1104646T>C
GRCh37.p13 chr 1 NC_000001.10:g.1040026= NC_000001.10:g.1040026T>C
C1orf159 transcript variant 1 NM_001330306.2:c.-136+10376= NM_001330306.2:c.-136+10376A>G
C1orf159 transcript variant 3 NM_001363525.2:c.-136+10376= NM_001363525.2:c.-136+10376A>G
C1orf159 transcript variant 2 NM_017891.4:c.-136+11414= NM_017891.4:c.-136+11414A>G
C1orf159 transcript variant 2 NM_017891.5:c.-136+11414= NM_017891.5:c.-136+11414A>G
C1orf159 transcript variant X1 XM_005244764.1:c.-136+10376= XM_005244764.1:c.-136+10376A>G
C1orf159 transcript variant X16 XM_005244765.1:c.-136+11414= XM_005244765.1:c.-136+11414A>G
C1orf159 transcript variant X3 XM_005244766.1:c.-136+11414= XM_005244766.1:c.-136+11414A>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#.

115 SubSNP, 23 Frequency submissions
No Submitter Submission ID Date (Build)
1 BCM_SSAHASNP ss9838867 Jul 11, 2003 (116)
2 CSHL-HAPMAP ss16407584 Feb 27, 2004 (120)
3 ABI ss43816996 Mar 15, 2006 (126)
4 ILLUMINA ss75226577 Dec 06, 2007 (129)
5 HGSV ss83884063 Dec 14, 2007 (130)
6 HGSV ss85461078 Dec 14, 2007 (130)
7 HUMANGENOME_JCVI ss99179714 Feb 04, 2009 (130)
8 BGI ss102713584 Dec 01, 2009 (131)
9 1000GENOMES ss109941096 Jan 24, 2009 (130)
10 KRIBB_YJKIM ss119520080 Dec 01, 2009 (131)
11 ENSEMBL ss131631867 Dec 01, 2009 (131)
12 ILLUMINA ss160796290 Dec 01, 2009 (131)
13 COMPLETE_GENOMICS ss162983269 Jul 04, 2010 (132)
14 COMPLETE_GENOMICS ss165982403 Jul 04, 2010 (132)
15 ILLUMINA ss174062980 Jul 04, 2010 (132)
16 BUSHMAN ss197888669 Jul 04, 2010 (132)
17 BCM-HGSC-SUB ss205443586 Jul 04, 2010 (132)
18 1000GENOMES ss218191817 Jul 14, 2010 (132)
19 1000GENOMES ss230396399 Jul 14, 2010 (132)
20 1000GENOMES ss238115948 Jul 15, 2010 (132)
21 GMI ss275682415 May 04, 2012 (137)
22 PJP ss290494330 May 09, 2011 (134)
23 ILLUMINA ss481311854 May 04, 2012 (137)
24 ILLUMINA ss481336910 May 04, 2012 (137)
25 ILLUMINA ss482319081 Sep 08, 2015 (146)
26 ILLUMINA ss485451113 May 04, 2012 (137)
27 ILLUMINA ss537376441 Sep 08, 2015 (146)
28 TISHKOFF ss553713355 Apr 25, 2013 (138)
29 SSMP ss647518326 Apr 25, 2013 (138)
30 ILLUMINA ss779046310 Aug 21, 2014 (142)
31 ILLUMINA ss783171005 Aug 21, 2014 (142)
32 ILLUMINA ss784126548 Aug 21, 2014 (142)
33 ILLUMINA ss832430548 Apr 01, 2015 (144)
34 ILLUMINA ss834509224 Aug 21, 2014 (142)
35 EVA-GONL ss974771863 Aug 21, 2014 (142)
36 JMKIDD_LAB ss1067613590 Aug 21, 2014 (142)
37 1000GENOMES ss1289349808 Aug 21, 2014 (142)
38 HAMMER_LAB ss1397238524 Sep 08, 2015 (146)
39 DDI ss1425685806 Apr 01, 2015 (144)
40 EVA_GENOME_DK ss1573851961 Apr 01, 2015 (144)
41 EVA_DECODE ss1584131798 Apr 01, 2015 (144)
42 EVA_UK10K_ALSPAC ss1599382353 Apr 01, 2015 (144)
43 EVA_UK10K_TWINSUK ss1642376386 Apr 01, 2015 (144)
44 EVA_SVP ss1712305545 Apr 01, 2015 (144)
45 ILLUMINA ss1751860415 Sep 08, 2015 (146)
46 HAMMER_LAB ss1793716765 Sep 08, 2015 (146)
47 WEILL_CORNELL_DGM ss1917963740 Feb 12, 2016 (147)
48 ILLUMINA ss1945981810 Feb 12, 2016 (147)
49 ILLUMINA ss1958230785 Feb 12, 2016 (147)
50 JJLAB ss2019499757 Sep 14, 2016 (149)
51 USC_VALOUEV ss2147486495 Dec 20, 2016 (150)
52 HUMAN_LONGEVITY ss2159385184 Dec 20, 2016 (150)
53 SYSTEMSBIOZJU ss2624265494 Nov 08, 2017 (151)
54 ILLUMINA ss2632465734 Nov 08, 2017 (151)
55 GRF ss2697377434 Nov 08, 2017 (151)
56 ILLUMINA ss2710663577 Nov 08, 2017 (151)
57 GNOMAD ss2750670438 Nov 08, 2017 (151)
58 SWEGEN ss2986154172 Nov 08, 2017 (151)
59 ILLUMINA ss3021043739 Nov 08, 2017 (151)
60 BIOINF_KMB_FNS_UNIBA ss3023514261 Nov 08, 2017 (151)
61 CSHL ss3343274187 Nov 08, 2017 (151)
62 ILLUMINA ss3625523509 Oct 11, 2018 (152)
63 ILLUMINA ss3626007081 Oct 11, 2018 (152)
64 ILLUMINA ss3630505779 Oct 11, 2018 (152)
65 ILLUMINA ss3632878063 Oct 11, 2018 (152)
66 ILLUMINA ss3633571483 Oct 11, 2018 (152)
67 ILLUMINA ss3634302069 Oct 11, 2018 (152)
68 ILLUMINA ss3635265686 Oct 11, 2018 (152)
69 ILLUMINA ss3635978719 Oct 11, 2018 (152)
70 ILLUMINA ss3637016026 Oct 11, 2018 (152)
71 ILLUMINA ss3637732497 Oct 11, 2018 (152)
72 ILLUMINA ss3640009435 Oct 11, 2018 (152)
73 ILLUMINA ss3640973171 Oct 11, 2018 (152)
74 ILLUMINA ss3641266986 Oct 11, 2018 (152)
75 ILLUMINA ss3642746772 Oct 11, 2018 (152)
76 ILLUMINA ss3644477673 Oct 11, 2018 (152)
77 URBANLAB ss3646581887 Oct 11, 2018 (152)
78 ILLUMINA ss3651365791 Oct 11, 2018 (152)
79 EGCUT_WGS ss3654265256 Jul 12, 2019 (153)
80 EVA_DECODE ss3685997726 Jul 12, 2019 (153)
81 ILLUMINA ss3724988463 Jul 12, 2019 (153)
82 ACPOP ss3726718588 Jul 12, 2019 (153)
83 ILLUMINA ss3744040779 Jul 12, 2019 (153)
84 ILLUMINA ss3744603000 Jul 12, 2019 (153)
85 EVA ss3745724160 Jul 12, 2019 (153)
86 PAGE_CC ss3770778832 Jul 12, 2019 (153)
87 ILLUMINA ss3772104758 Jul 12, 2019 (153)
88 KHV_HUMAN_GENOMES ss3798746755 Jul 12, 2019 (153)
89 EVA ss3825982554 Apr 25, 2020 (154)
90 SGDP_PRJ ss3848003568 Apr 25, 2020 (154)
91 KRGDB ss3892846307 Apr 25, 2020 (154)
92 KOGIC ss3943635979 Apr 25, 2020 (154)
93 EVA ss3984450758 Apr 25, 2021 (155)
94 EVA ss4016889115 Apr 25, 2021 (155)
95 TOPMED ss4436516343 Apr 25, 2021 (155)
96 TOMMO_GENOMICS ss5142066268 Apr 25, 2021 (155)
97 EVA ss5237258275 Apr 25, 2021 (155)
98 1000G_HIGH_COVERAGE ss5240873058 Oct 12, 2022 (156)
99 EVA ss5314586044 Oct 12, 2022 (156)
100 EVA ss5316199298 Oct 12, 2022 (156)
101 HUGCELL_USP ss5442119925 Oct 12, 2022 (156)
102 EVA ss5505748368 Oct 12, 2022 (156)
103 1000G_HIGH_COVERAGE ss5512501650 Oct 12, 2022 (156)
104 SANFORD_IMAGENETICS ss5624193878 Oct 12, 2022 (156)
105 SANFORD_IMAGENETICS ss5624755062 Oct 12, 2022 (156)
106 TOMMO_GENOMICS ss5666210545 Oct 12, 2022 (156)
107 EVA ss5799472573 Oct 12, 2022 (156)
108 YY_MCH ss5800246224 Oct 12, 2022 (156)
109 EVA ss5831422641 Oct 12, 2022 (156)
110 EVA ss5847150767 Oct 12, 2022 (156)
111 EVA ss5847521466 Oct 12, 2022 (156)
112 EVA ss5848749723 Oct 12, 2022 (156)
113 EVA ss5906714462 Oct 12, 2022 (156)
114 EVA ss5936587391 Oct 12, 2022 (156)
115 EVA ss5979259880 Oct 12, 2022 (156)
116 1000Genomes NC_000001.10 - 1040026 Oct 11, 2018 (152)
117 1000Genomes_30x NC_000001.11 - 1104646 Oct 12, 2022 (156)
118 The Avon Longitudinal Study of Parents and Children NC_000001.10 - 1040026 Oct 11, 2018 (152)
119 Genome-wide autozygosity in Daghestan NC_000001.9 - 1029889 Apr 25, 2020 (154)
120 Genetic variation in the Estonian population NC_000001.10 - 1040026 Oct 11, 2018 (152)
121 The Danish reference pan genome NC_000001.10 - 1040026 Apr 25, 2020 (154)
122 gnomAD - Genomes NC_000001.11 - 1104646 Apr 25, 2021 (155)
123 Genome of the Netherlands Release 5 NC_000001.10 - 1040026 Apr 25, 2020 (154)
124 HapMap NC_000001.11 - 1104646 Apr 25, 2020 (154)
125 KOREAN population from KRGDB NC_000001.10 - 1040026 Apr 25, 2020 (154)
126 Korean Genome Project NC_000001.11 - 1104646 Apr 25, 2020 (154)
127 Northern Sweden NC_000001.10 - 1040026 Jul 12, 2019 (153)
128 The PAGE Study NC_000001.11 - 1104646 Jul 12, 2019 (153)
129 CNV burdens in cranial meningiomas NC_000001.10 - 1040026 Apr 25, 2021 (155)
130 Qatari NC_000001.10 - 1040026 Apr 25, 2020 (154)
131 SGDP_PRJ NC_000001.10 - 1040026 Apr 25, 2020 (154)
132 Siberian NC_000001.10 - 1040026 Apr 25, 2020 (154)
133 8.3KJPN NC_000001.10 - 1040026 Apr 25, 2021 (155)
134 14KJPN NC_000001.11 - 1104646 Oct 12, 2022 (156)
135 TopMed NC_000001.11 - 1104646 Apr 25, 2021 (155)
136 UK 10K study - Twins NC_000001.10 - 1040026 Oct 11, 2018 (152)
137 A Vietnamese Genetic Variation Database NC_000001.10 - 1040026 Jul 12, 2019 (153)
138 ALFA NC_000001.11 - 1104646 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)
rs57669203 May 24, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss83884063, ss85461078 NC_000001.8:1079948:T:C NC_000001.11:1104645:T:C (self)
11, ss109941096, ss160796290, ss162983269, ss165982403, ss197888669, ss205443586, ss275682415, ss290494330, ss481311854, ss1397238524, ss1584131798, ss1712305545, ss3642746772 NC_000001.9:1029888:T:C NC_000001.11:1104645:T:C (self)
14918, 4717, 3504, 1359195, 2199, 23701, 3453, 57, 5670, 20548, 2849, 35575, 4717, 1056, ss218191817, ss230396399, ss238115948, ss481336910, ss482319081, ss485451113, ss537376441, ss553713355, ss647518326, ss779046310, ss783171005, ss784126548, ss832430548, ss834509224, ss974771863, ss1067613590, ss1289349808, ss1425685806, ss1573851961, ss1599382353, ss1642376386, ss1751860415, ss1793716765, ss1917963740, ss1945981810, ss1958230785, ss2019499757, ss2147486495, ss2624265494, ss2632465734, ss2697377434, ss2710663577, ss2750670438, ss2986154172, ss3021043739, ss3343274187, ss3625523509, ss3626007081, ss3630505779, ss3632878063, ss3633571483, ss3634302069, ss3635265686, ss3635978719, ss3637016026, ss3637732497, ss3640009435, ss3640973171, ss3641266986, ss3644477673, ss3651365791, ss3654265256, ss3726718588, ss3744040779, ss3744603000, ss3745724160, ss3772104758, ss3825982554, ss3848003568, ss3892846307, ss3984450758, ss4016889115, ss5142066268, ss5237258275, ss5314586044, ss5316199298, ss5505748368, ss5624193878, ss5624755062, ss5799472573, ss5831422641, ss5847150767, ss5847521466, ss5936587391, ss5979259880 NC_000001.10:1040025:T:C NC_000001.11:1104645:T:C (self)
27585, 138355, 211, 13980, 301, 47649, 122678, 3483399670, ss2159385184, ss3023514261, ss3646581887, ss3685997726, ss3724988463, ss3770778832, ss3798746755, ss3943635979, ss4436516343, ss5240873058, ss5442119925, ss5512501650, ss5666210545, ss5800246224, ss5848749723, ss5906714462 NC_000001.11:1104645:T:C NC_000001.11:1104645:T:C (self)
ss43816996, ss75226577, ss99179714, ss102713584, ss119520080, ss131631867, ss174062980 NT_004350.19:518657:T:C NC_000001.11:1104645:T:C (self)
ss16407584 NT_077913.2:43736:T:C NC_000001.11:1104645:T:C (self)
ss9838867 NT_077960.1:109466:T:C NC_000001.11:1104645:T: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 rs6671356

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