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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.

rs6702935

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr1:3816143 (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>C
Variation Type
SNV Single Nucleotide Variation
Frequency
T=0.352677 (93350/264690, TOPMED)
T=0.349734 (48974/140032, GnomAD)
T=0.41578 (34236/82342, ALFA) (+ 19 more)
C=0.44553 (7467/16760, 8.3KJPN)
T=0.3437 (1721/5008, 1000G)
T=0.4339 (1944/4480, Estonian)
T=0.4510 (1738/3854, ALSPAC)
T=0.4569 (1694/3708, TWINSUK)
T=0.4573 (1340/2930, KOREAN)
T=0.3925 (818/2084, HGDP_Stanford)
T=0.3077 (581/1888, HapMap)
T=0.4307 (789/1832, Korea1K)
T=0.440 (439/998, GoNL)
C=0.462 (289/626, Chileans)
T=0.458 (275/600, NorthernSweden)
C=0.191 (102/534, MGP)
T=0.240 (109/454, SGDP_PRJ)
T=0.315 (68/216, Qatari)
T=0.335 (71/212, Vietnamese)
C=0.48 (42/88, Ancient Sardinia)
T=0.20 (10/50, Siberian)
T=0.40 (16/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
CEP104 : Intron Variant
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.3816143T>C
GRCh37.p13 chr 1 NC_000001.10:g.3732707T>C
CEP104 RefSeqGene NG_046726.1:g.46091A>G
Gene: CEP104, centrosomal protein 104 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
CEP104 transcript NM_014704.4:c.2662+137A>G N/A Intron Variant
CEP104 transcript variant X2 XM_005244815.4:c.2770+137…

XM_005244815.4:c.2770+137A>G

N/A Intron Variant
CEP104 transcript variant X3 XM_011542474.3:c.2680+137…

XM_011542474.3:c.2680+137A>G

N/A Intron Variant
CEP104 transcript variant X7 XM_017002918.2:c.2488+137…

XM_017002918.2:c.2488+137A>G

N/A Intron Variant
CEP104 transcript variant X8 XM_017002919.2:c.2464+137…

XM_017002919.2:c.2464+137A>G

N/A Intron Variant
CEP104 transcript variant X1 XM_024451101.1:c.2788+137…

XM_024451101.1:c.2788+137A>G

N/A Intron Variant
CEP104 transcript variant X4 XM_024451102.1:c.2614+137…

XM_024451102.1:c.2614+137A>G

N/A Intron Variant
CEP104 transcript variant X5 XM_024451103.1:c.2596+137…

XM_024451103.1:c.2596+137A>G

N/A Intron Variant
CEP104 transcript variant X6 XM_024451104.1:c.2590+137…

XM_024451104.1:c.2590+137A>G

N/A Intron Variant
CEP104 transcript variant X9 XM_024451106.1:c.2416+137…

XM_024451106.1:c.2416+137A>G

N/A Intron Variant
CEP104 transcript variant X10 XM_024451108.1:c. N/A Genic Downstream 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

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 82342 T=0.41578 C=0.58422
European Sub 65808 T=0.44203 C=0.55797
African Sub 5202 T=0.1348 C=0.8652
African Others Sub 182 T=0.060 C=0.940
African American Sub 5020 T=0.1375 C=0.8625
Asian Sub 238 T=0.521 C=0.479
East Asian Sub 164 T=0.488 C=0.512
Other Asian Sub 74 T=0.59 C=0.41
Latin American 1 Sub 400 T=0.378 C=0.623
Latin American 2 Sub 3392 T=0.4782 C=0.5218
South Asian Sub 4968 T=0.3219 C=0.6781
Other Sub 2334 T=0.4070 C=0.5930


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=0.352677 C=0.647323
gnomAD - Genomes Global Study-wide 140032 T=0.349734 C=0.650266
gnomAD - Genomes European Sub 75834 T=0.43552 C=0.56448
gnomAD - Genomes African Sub 41962 T=0.14258 C=0.85742
gnomAD - Genomes American Sub 13638 T=0.49061 C=0.50939
gnomAD - Genomes Ashkenazi Jewish Sub 3318 T=0.3421 C=0.6579
gnomAD - Genomes East Asian Sub 3128 T=0.4198 C=0.5802
gnomAD - Genomes Other Sub 2152 T=0.3834 C=0.6166
8.3KJPN JAPANESE Study-wide 16760 T=0.55447 C=0.44553
1000Genomes Global Study-wide 5008 T=0.3437 C=0.6563
1000Genomes African Sub 1322 T=0.0862 C=0.9138
1000Genomes East Asian Sub 1008 T=0.4266 C=0.5734
1000Genomes Europe Sub 1006 T=0.4573 C=0.5427
1000Genomes South Asian Sub 978 T=0.351 C=0.649
1000Genomes American Sub 694 T=0.539 C=0.461
Genetic variation in the Estonian population Estonian Study-wide 4480 T=0.4339 C=0.5661
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 T=0.4510 C=0.5490
UK 10K study - Twins TWIN COHORT Study-wide 3708 T=0.4569 C=0.5431
KOREAN population from KRGDB KOREAN Study-wide 2930 T=0.4573 C=0.5427
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 T=0.3925 C=0.6075
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 T=0.430 C=0.570
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 T=0.297 C=0.703
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 T=0.411 C=0.589
HGDP-CEPH-db Supplement 1 Europe Sub 320 T=0.453 C=0.547
HGDP-CEPH-db Supplement 1 Africa Sub 242 T=0.095 C=0.905
HGDP-CEPH-db Supplement 1 America Sub 216 T=0.657 C=0.343
HGDP-CEPH-db Supplement 1 Oceania Sub 72 T=0.54 C=0.46
HapMap Global Study-wide 1888 T=0.3077 C=0.6923
HapMap American Sub 770 T=0.412 C=0.588
HapMap African Sub 688 T=0.090 C=0.910
HapMap Asian Sub 254 T=0.488 C=0.512
HapMap Europe Sub 176 T=0.443 C=0.557
Korean Genome Project KOREAN Study-wide 1832 T=0.4307 C=0.5693
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 T=0.440 C=0.560
Chileans Chilean Study-wide 626 T=0.538 C=0.462
Northern Sweden ACPOP Study-wide 600 T=0.458 C=0.542
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 T=0.809 C=0.191
SGDP_PRJ Global Study-wide 454 T=0.240 C=0.760
Qatari Global Study-wide 216 T=0.315 C=0.685
A Vietnamese Genetic Variation Database Global Study-wide 212 T=0.335 C=0.665
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 88 T=0.52 C=0.48
Siberian Global Study-wide 50 T=0.20 C=0.80
The Danish reference pan genome Danish Study-wide 40 T=0.40 C=0.60
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.p13 chr 1 NC_000001.11:g.3816143= NC_000001.11:g.3816143T>C
GRCh37.p13 chr 1 NC_000001.10:g.3732707= NC_000001.10:g.3732707T>C
CEP104 RefSeqGene NG_046726.1:g.46091= NG_046726.1:g.46091A>G
CEP104 transcript NM_014704.3:c.2662+137= NM_014704.3:c.2662+137A>G
CEP104 transcript NM_014704.4:c.2662+137= NM_014704.4:c.2662+137A>G
CEP104 transcript variant X1 XM_005244815.1:c.2770+137= XM_005244815.1:c.2770+137A>G
CEP104 transcript variant X2 XM_005244815.4:c.2770+137= XM_005244815.4:c.2770+137A>G
CEP104 transcript variant X3 XM_011542474.3:c.2680+137= XM_011542474.3:c.2680+137A>G
CEP104 transcript variant X7 XM_017002918.2:c.2488+137= XM_017002918.2:c.2488+137A>G
CEP104 transcript variant X8 XM_017002919.2:c.2464+137= XM_017002919.2:c.2464+137A>G
CEP104 transcript variant X1 XM_024451101.1:c.2788+137= XM_024451101.1:c.2788+137A>G
CEP104 transcript variant X4 XM_024451102.1:c.2614+137= XM_024451102.1:c.2614+137A>G
CEP104 transcript variant X5 XM_024451103.1:c.2596+137= XM_024451103.1:c.2596+137A>G
CEP104 transcript variant X6 XM_024451104.1:c.2590+137= XM_024451104.1:c.2590+137A>G
CEP104 transcript variant X9 XM_024451106.1:c.2416+137= XM_024451106.1:c.2416+137A>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#.

107 SubSNP, 22 Frequency submissions
No Submitter Submission ID Date (Build)
1 BCM_SSAHASNP ss9903476 Jul 11, 2003 (116)
2 SC_SNP ss12992572 Dec 05, 2003 (119)
3 SSAHASNP ss20600937 Apr 05, 2004 (121)
4 PERLEGEN ss24243547 Sep 20, 2004 (123)
5 ABI ss44054264 Mar 15, 2006 (126)
6 AFFY ss66181834 Dec 01, 2006 (127)
7 ILLUMINA ss66623462 Dec 01, 2006 (127)
8 ILLUMINA ss67486911 Dec 01, 2006 (127)
9 ILLUMINA ss67845117 Dec 01, 2006 (127)
10 ILLUMINA ss70880683 May 25, 2008 (130)
11 ILLUMINA ss71471327 May 18, 2007 (127)
12 ILLUMINA ss75468009 Dec 07, 2007 (129)
13 AFFY ss76247708 Dec 07, 2007 (129)
14 SI_EXO ss76890951 Dec 07, 2007 (129)
15 HGSV ss78660593 Dec 07, 2007 (129)
16 ILLUMINA ss79230368 Dec 15, 2007 (130)
17 HGSV ss82133683 Dec 15, 2007 (130)
18 KRIBB_YJKIM ss84527073 Dec 15, 2007 (130)
19 HGSV ss84529098 Dec 15, 2007 (130)
20 HUMANGENOME_JCVI ss97915487 Feb 05, 2009 (130)
21 BGI ss106560643 Feb 05, 2009 (130)
22 1000GENOMES ss107949035 Jan 22, 2009 (130)
23 1000GENOMES ss109967481 Jan 24, 2009 (130)
24 ILLUMINA-UK ss118453506 Feb 14, 2009 (130)
25 ILLUMINA ss122597563 Dec 01, 2009 (131)
26 ENSEMBL ss131785234 Dec 01, 2009 (131)
27 ILLUMINA ss154376427 Dec 01, 2009 (131)
28 ILLUMINA ss159552286 Dec 01, 2009 (131)
29 COMPLETE_GENOMICS ss163004852 Jul 04, 2010 (132)
30 COMPLETE_GENOMICS ss163738108 Jul 04, 2010 (132)
31 ILLUMINA ss172174891 Jul 04, 2010 (132)
32 AFFY ss172965238 Jul 04, 2010 (132)
33 ILLUMINA ss174076185 Jul 04, 2010 (132)
34 BUSHMAN ss197925061 Jul 04, 2010 (132)
35 BCM-HGSC-SUB ss205105233 Jul 04, 2010 (132)
36 1000GENOMES ss218203274 Jul 14, 2010 (132)
37 1000GENOMES ss230404157 Jul 14, 2010 (132)
38 1000GENOMES ss238123040 Jul 15, 2010 (132)
39 BL ss252880411 May 09, 2011 (134)
40 GMI ss275691459 May 04, 2012 (137)
41 GMI ss283991015 Apr 25, 2013 (138)
42 PJP ss290498322 May 09, 2011 (134)
43 ILLUMINA ss537380767 Sep 08, 2015 (146)
44 TISHKOFF ss553734706 Apr 25, 2013 (138)
45 SSMP ss647536491 Apr 25, 2013 (138)
46 ILLUMINA ss825560886 Apr 01, 2015 (144)
47 ILLUMINA ss833063458 Aug 21, 2014 (142)
48 ILLUMINA ss833654286 Aug 21, 2014 (142)
49 EVA-GONL ss974796486 Aug 21, 2014 (142)
50 JMKIDD_LAB ss1067627320 Aug 21, 2014 (142)
51 1000GENOMES ss1289451801 Aug 21, 2014 (142)
52 DDI ss1425693018 Apr 01, 2015 (144)
53 EVA_GENOME_DK ss1573860153 Apr 01, 2015 (144)
54 EVA_DECODE ss1584155265 Apr 01, 2015 (144)
55 EVA_UK10K_ALSPAC ss1599427420 Apr 01, 2015 (144)
56 EVA_UK10K_TWINSUK ss1642421453 Apr 01, 2015 (144)
57 EVA_MGP ss1710885663 Apr 01, 2015 (144)
58 EVA_SVP ss1712306776 Apr 01, 2015 (144)
59 HAMMER_LAB ss1793785134 Sep 08, 2015 (146)
60 WEILL_CORNELL_DGM ss1917992022 Feb 12, 2016 (147)
61 GENOMED ss1966671383 Jul 19, 2016 (147)
62 JJLAB ss2019512161 Sep 14, 2016 (149)
63 USC_VALOUEV ss2147502541 Dec 20, 2016 (150)
64 HUMAN_LONGEVITY ss2159574887 Dec 20, 2016 (150)
65 TOPMED ss2321729836 Dec 20, 2016 (150)
66 SYSTEMSBIOZJU ss2624271838 Nov 08, 2017 (151)
67 GRF ss2697396574 Nov 08, 2017 (151)
68 GNOMAD ss2750972645 Nov 08, 2017 (151)
69 AFFY ss2984842610 Nov 08, 2017 (151)
70 AFFY ss2985497054 Nov 08, 2017 (151)
71 SWEGEN ss2986201372 Nov 08, 2017 (151)
72 BIOINF_KMB_FNS_UNIBA ss3023519701 Nov 08, 2017 (151)
73 TOPMED ss3067127283 Nov 08, 2017 (151)
74 CSHL ss3343288964 Nov 08, 2017 (151)
75 ILLUMINA ss3626011925 Oct 11, 2018 (152)
76 ILLUMINA ss3637733769 Oct 11, 2018 (152)
77 ILLUMINA ss3638888277 Oct 11, 2018 (152)
78 ILLUMINA ss3639440885 Oct 11, 2018 (152)
79 ILLUMINA ss3640973634 Oct 11, 2018 (152)
80 ILLUMINA ss3641267448 Oct 11, 2018 (152)
81 ILLUMINA ss3642747980 Oct 11, 2018 (152)
82 URBANLAB ss3646586760 Oct 11, 2018 (152)
83 ILLUMINA ss3653616410 Oct 11, 2018 (152)
84 EGCUT_WGS ss3654302596 Jul 12, 2019 (153)
85 EVA_DECODE ss3686047268 Jul 12, 2019 (153)
86 ACPOP ss3726740070 Jul 12, 2019 (153)
87 EVA ss3745755374 Jul 12, 2019 (153)
88 PACBIO ss3783308794 Jul 12, 2019 (153)
89 PACBIO ss3788985675 Jul 12, 2019 (153)
90 PACBIO ss3793858305 Jul 12, 2019 (153)
91 KHV_HUMAN_GENOMES ss3798777053 Jul 12, 2019 (153)
92 EVA ss3825551291 Apr 25, 2020 (154)
93 EVA ss3825993990 Apr 25, 2020 (154)
94 EVA ss3836384171 Apr 25, 2020 (154)
95 EVA ss3841788335 Apr 25, 2020 (154)
96 HGDP ss3847322569 Apr 25, 2020 (154)
97 SGDP_PRJ ss3848069592 Apr 25, 2020 (154)
98 KRGDB ss3892931171 Apr 25, 2020 (154)
99 KOGIC ss3943692959 Apr 25, 2020 (154)
100 FSA-LAB ss3983913130 Apr 25, 2021 (155)
101 FSA-LAB ss3983913131 Apr 25, 2021 (155)
102 EVA ss3984774945 Apr 25, 2021 (155)
103 EVA ss3986095366 Apr 25, 2021 (155)
104 EVA ss4016890111 Apr 25, 2021 (155)
105 TOPMED ss4437306405 Apr 25, 2021 (155)
106 TOMMO_GENOMICS ss5142201826 Apr 25, 2021 (155)
107 EVA ss5237158799 Apr 25, 2021 (155)
108 1000Genomes NC_000001.10 - 3732707 Oct 11, 2018 (152)
109 The Avon Longitudinal Study of Parents and Children NC_000001.10 - 3732707 Oct 11, 2018 (152)
110 Chileans NC_000001.10 - 3732707 Apr 25, 2020 (154)
111 Genetic variation in the Estonian population NC_000001.10 - 3732707 Oct 11, 2018 (152)
112 The Danish reference pan genome NC_000001.10 - 3732707 Apr 25, 2020 (154)
113 gnomAD - Genomes NC_000001.11 - 3816143 Apr 25, 2021 (155)
114 Genome of the Netherlands Release 5 NC_000001.10 - 3732707 Apr 25, 2020 (154)
115 HGDP-CEPH-db Supplement 1 NC_000001.9 - 3722567 Apr 25, 2020 (154)
116 HapMap NC_000001.11 - 3816143 Apr 25, 2020 (154)
117 KOREAN population from KRGDB NC_000001.10 - 3732707 Apr 25, 2020 (154)
118 Korean Genome Project NC_000001.11 - 3816143 Apr 25, 2020 (154)
119 Medical Genome Project healthy controls from Spanish population NC_000001.10 - 3732707 Apr 25, 2020 (154)
120 Northern Sweden NC_000001.10 - 3732707 Jul 12, 2019 (153)
121 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000001.10 - 3732707 Apr 25, 2021 (155)
122 Qatari NC_000001.10 - 3732707 Apr 25, 2020 (154)
123 SGDP_PRJ NC_000001.10 - 3732707 Apr 25, 2020 (154)
124 Siberian NC_000001.10 - 3732707 Apr 25, 2020 (154)
125 8.3KJPN NC_000001.10 - 3732707 Apr 25, 2021 (155)
126 TopMed NC_000001.11 - 3816143 Apr 25, 2021 (155)
127 UK 10K study - Twins NC_000001.10 - 3732707 Oct 11, 2018 (152)
128 A Vietnamese Genetic Variation Database NC_000001.10 - 3732707 Jul 12, 2019 (153)
129 ALFA NC_000001.11 - 3816143 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)
rs17411729 Oct 07, 2004 (123)
rs59775655 May 25, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss78660593, ss82133683, ss84529098, ss3638888277, ss3639440885 NC_000001.8:3755863:T:C NC_000001.11:3816142:T:C (self)
461, ss66181834, ss76247708, ss107949035, ss109967481, ss118453506, ss163004852, ss163738108, ss172965238, ss197925061, ss205105233, ss252880411, ss275691459, ss283991015, ss290498322, ss825560886, ss1584155265, ss1712306776, ss3642747980, ss3847322569 NC_000001.9:3722566:T:C NC_000001.11:3816142:T:C (self)
119832, 53665, 239, 40844, 1367387, 23092, 108565, 2415, 24935, 872, 33952, 86572, 18895, 171133, 53665, 11342, ss218203274, ss230404157, ss238123040, ss537380767, ss553734706, ss647536491, ss833063458, ss833654286, ss974796486, ss1067627320, ss1289451801, ss1425693018, ss1573860153, ss1599427420, ss1642421453, ss1710885663, ss1793785134, ss1917992022, ss1966671383, ss2019512161, ss2147502541, ss2321729836, ss2624271838, ss2697396574, ss2750972645, ss2984842610, ss2985497054, ss2986201372, ss3343288964, ss3626011925, ss3637733769, ss3640973634, ss3641267448, ss3653616410, ss3654302596, ss3726740070, ss3745755374, ss3783308794, ss3788985675, ss3793858305, ss3825551291, ss3825993990, ss3836384171, ss3848069592, ss3892931171, ss3983913130, ss3983913131, ss3984774945, ss3986095366, ss4016890111, ss5142201826 NC_000001.10:3732706:T:C NC_000001.11:3816142:T:C (self)
864350, 2810, 70960, 568228, 912740, 3483166801, ss2159574887, ss3023519701, ss3067127283, ss3646586760, ss3686047268, ss3798777053, ss3841788335, ss3943692959, ss4437306405, ss5237158799 NC_000001.11:3816142:T:C NC_000001.11:3816142:T:C (self)
ss9903476, ss12992572, ss20600937 NT_004321.15:1039480:T:C NC_000001.11:3816142:T:C (self)
ss76890951 NT_004321.17:1048486:T:C NC_000001.11:3816142:T:C (self)
ss24243547, ss44054264, ss66623462, ss67486911, ss67845117, ss70880683, ss71471327, ss75468009, ss79230368, ss84527073, ss97915487, ss106560643, ss122597563, ss131785234, ss154376427, ss159552286, ss172174891, ss174076185 NT_004350.19:3211338:T:C NC_000001.11:3816142: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 rs6702935

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