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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.

rs6703035

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr1:3816218 (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=0.330674 (87526/264690, TOPMED)
T=0.329484 (46166/140116, GnomAD)
T=0.360770 (44366/122976, GnomAD_exome) (+ 17 more)
T=0.37616 (13040/34666, ALFA)
T=0.32178 (5718/17770, ExAC)
T=0.43699 (7324/16760, 8.3KJPN)
T=0.3085 (1545/5008, 1000G)
T=0.4000 (1792/4480, Estonian)
T=0.4338 (1672/3854, ALSPAC)
T=0.4385 (1626/3708, TWINSUK)
T=0.3444 (1009/2930, KOREAN)
T=0.2704 (511/1890, HapMap)
T=0.415 (414/998, GoNL)
T=0.438 (263/600, NorthernSweden)
T=0.485 (259/534, MGP)
T=0.228 (110/482, SGDP_PRJ)
T=0.255 (55/216, Qatari)
T=0.276 (58/210, Vietnamese)
T=0.21 (10/48, Siberian)
T=0.35 (14/40, 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.3816218T>A
GRCh38.p13 chr 1 NC_000001.11:g.3816218T>C
GRCh38.p13 chr 1 NC_000001.11:g.3816218T>G
GRCh37.p13 chr 1 NC_000001.10:g.3732782T>A
GRCh37.p13 chr 1 NC_000001.10:g.3732782T>C
GRCh37.p13 chr 1 NC_000001.10:g.3732782T>G
CEP104 RefSeqGene NG_046726.1:g.46016A>T
CEP104 RefSeqGene NG_046726.1:g.46016A>G
CEP104 RefSeqGene NG_046726.1:g.46016A>C
Gene: CEP104, centrosomal protein 104 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
CEP104 transcript NM_014704.4:c.2662+62A>T N/A Intron Variant
CEP104 transcript variant X2 XM_005244815.4:c.2770+62A…

XM_005244815.4:c.2770+62A>T

N/A Intron Variant
CEP104 transcript variant X3 XM_011542474.3:c.2680+62A…

XM_011542474.3:c.2680+62A>T

N/A Intron Variant
CEP104 transcript variant X7 XM_017002918.2:c.2488+62A…

XM_017002918.2:c.2488+62A>T

N/A Intron Variant
CEP104 transcript variant X8 XM_017002919.2:c.2464+62A…

XM_017002919.2:c.2464+62A>T

N/A Intron Variant
CEP104 transcript variant X1 XM_024451101.1:c.2788+62A…

XM_024451101.1:c.2788+62A>T

N/A Intron Variant
CEP104 transcript variant X4 XM_024451102.1:c.2614+62A…

XM_024451102.1:c.2614+62A>T

N/A Intron Variant
CEP104 transcript variant X5 XM_024451103.1:c.2596+62A…

XM_024451103.1:c.2596+62A>T

N/A Intron Variant
CEP104 transcript variant X6 XM_024451104.1:c.2590+62A…

XM_024451104.1:c.2590+62A>T

N/A Intron Variant
CEP104 transcript variant X9 XM_024451106.1:c.2416+62A…

XM_024451106.1:c.2416+62A>T

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 34666 T=0.37616 C=0.62384
European Sub 23452 T=0.41216 C=0.58784
African Sub 4214 T=0.1540 C=0.8460
African Others Sub 134 T=0.052 C=0.948
African American Sub 4080 T=0.1574 C=0.8426
Asian Sub 216 T=0.343 C=0.657
East Asian Sub 128 T=0.305 C=0.695
Other Asian Sub 88 T=0.40 C=0.60
Latin American 1 Sub 290 T=0.331 C=0.669
Latin American 2 Sub 2770 T=0.4188 C=0.5812
South Asian Sub 110 T=0.236 C=0.764
Other Sub 3614 T=0.3788 C=0.6212


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=0.330674 C=0.669326
gnomAD - Genomes Global Study-wide 140116 T=0.329484 C=0.670516
gnomAD - Genomes European Sub 75868 T=0.41340 C=0.58660
gnomAD - Genomes African Sub 41994 T=0.13735 C=0.86265
gnomAD - Genomes American Sub 13654 T=0.45064 C=0.54936
gnomAD - Genomes Ashkenazi Jewish Sub 3324 T=0.3366 C=0.6634
gnomAD - Genomes East Asian Sub 3126 T=0.3199 C=0.6801
gnomAD - Genomes Other Sub 2150 T=0.3544 C=0.6456
gnomAD - Exomes Global Study-wide 122976 T=0.360770 C=0.639230
gnomAD - Exomes European Sub 60412 T=0.40159 C=0.59841
gnomAD - Exomes Asian Sub 26404 T=0.30458 C=0.69542
gnomAD - Exomes American Sub 19256 T=0.41410 C=0.58590
gnomAD - Exomes African Sub 7612 T=0.1239 C=0.8761
gnomAD - Exomes Ashkenazi Jewish Sub 5846 T=0.3178 C=0.6822
gnomAD - Exomes Other Sub 3446 T=0.3738 C=0.6262
ExAC Global Study-wide 17770 T=0.32178 C=0.67822
ExAC Europe Sub 9246 T=0.3927 C=0.6073
ExAC Asian Sub 5264 T=0.2876 C=0.7124
ExAC African Sub 2688 T=0.1324 C=0.8676
ExAC American Sub 366 T=0.407 C=0.593
ExAC Other Sub 206 T=0.330 C=0.670
8.3KJPN JAPANESE Study-wide 16760 T=0.43699 C=0.56301
1000Genomes Global Study-wide 5008 T=0.3085 C=0.6915
1000Genomes African Sub 1322 T=0.0825 C=0.9175
1000Genomes East Asian Sub 1008 T=0.3383 C=0.6617
1000Genomes Europe Sub 1006 T=0.4284 C=0.5716
1000Genomes South Asian Sub 978 T=0.331 C=0.669
1000Genomes American Sub 694 T=0.490 C=0.510
Genetic variation in the Estonian population Estonian Study-wide 4480 T=0.4000 C=0.6000
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 T=0.4338 C=0.5662
UK 10K study - Twins TWIN COHORT Study-wide 3708 T=0.4385 C=0.5615
KOREAN population from KRGDB KOREAN Study-wide 2930 T=0.3444 A=0.0000, C=0.6556, G=0.0000
HapMap Global Study-wide 1890 T=0.2704 C=0.7296
HapMap American Sub 768 T=0.368 C=0.632
HapMap African Sub 692 T=0.082 C=0.918
HapMap Asian Sub 254 T=0.398 C=0.602
HapMap Europe Sub 176 T=0.398 C=0.602
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 T=0.415 C=0.585
Northern Sweden ACPOP Study-wide 600 T=0.438 C=0.562
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 T=0.485 C=0.515
SGDP_PRJ Global Study-wide 482 T=0.228 C=0.772
Qatari Global Study-wide 216 T=0.255 C=0.745
A Vietnamese Genetic Variation Database Global Study-wide 210 T=0.276 C=0.724
Siberian Global Study-wide 48 T=0.21 C=0.79
The Danish reference pan genome Danish Study-wide 40 T=0.35 C=0.65
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.3816218= NC_000001.11:g.3816218T>A NC_000001.11:g.3816218T>C NC_000001.11:g.3816218T>G
GRCh37.p13 chr 1 NC_000001.10:g.3732782= NC_000001.10:g.3732782T>A NC_000001.10:g.3732782T>C NC_000001.10:g.3732782T>G
CEP104 RefSeqGene NG_046726.1:g.46016= NG_046726.1:g.46016A>T NG_046726.1:g.46016A>G NG_046726.1:g.46016A>C
CEP104 transcript NM_014704.3:c.2662+62= NM_014704.3:c.2662+62A>T NM_014704.3:c.2662+62A>G NM_014704.3:c.2662+62A>C
CEP104 transcript NM_014704.4:c.2662+62= NM_014704.4:c.2662+62A>T NM_014704.4:c.2662+62A>G NM_014704.4:c.2662+62A>C
CEP104 transcript variant X1 XM_005244815.1:c.2770+62= XM_005244815.1:c.2770+62A>T XM_005244815.1:c.2770+62A>G XM_005244815.1:c.2770+62A>C
CEP104 transcript variant X2 XM_005244815.4:c.2770+62= XM_005244815.4:c.2770+62A>T XM_005244815.4:c.2770+62A>G XM_005244815.4:c.2770+62A>C
CEP104 transcript variant X3 XM_011542474.3:c.2680+62= XM_011542474.3:c.2680+62A>T XM_011542474.3:c.2680+62A>G XM_011542474.3:c.2680+62A>C
CEP104 transcript variant X7 XM_017002918.2:c.2488+62= XM_017002918.2:c.2488+62A>T XM_017002918.2:c.2488+62A>G XM_017002918.2:c.2488+62A>C
CEP104 transcript variant X8 XM_017002919.2:c.2464+62= XM_017002919.2:c.2464+62A>T XM_017002919.2:c.2464+62A>G XM_017002919.2:c.2464+62A>C
CEP104 transcript variant X1 XM_024451101.1:c.2788+62= XM_024451101.1:c.2788+62A>T XM_024451101.1:c.2788+62A>G XM_024451101.1:c.2788+62A>C
CEP104 transcript variant X4 XM_024451102.1:c.2614+62= XM_024451102.1:c.2614+62A>T XM_024451102.1:c.2614+62A>G XM_024451102.1:c.2614+62A>C
CEP104 transcript variant X5 XM_024451103.1:c.2596+62= XM_024451103.1:c.2596+62A>T XM_024451103.1:c.2596+62A>G XM_024451103.1:c.2596+62A>C
CEP104 transcript variant X6 XM_024451104.1:c.2590+62= XM_024451104.1:c.2590+62A>T XM_024451104.1:c.2590+62A>G XM_024451104.1:c.2590+62A>C
CEP104 transcript variant X9 XM_024451106.1:c.2416+62= XM_024451106.1:c.2416+62A>T XM_024451106.1:c.2416+62A>G XM_024451106.1:c.2416+62A>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#.

85 SubSNP, 20 Frequency submissions
No Submitter Submission ID Date (Build)
1 BCM_SSAHASNP ss9903675 Jul 11, 2003 (116)
2 SC_SNP ss12992573 Dec 05, 2003 (119)
3 CSHL-HAPMAP ss19851002 Feb 27, 2004 (120)
4 SSAHASNP ss20601694 Apr 05, 2004 (121)
5 PERLEGEN ss24243551 Sep 20, 2004 (123)
6 ABI ss44124923 Mar 13, 2006 (126)
7 SI_EXO ss61706815 Oct 14, 2006 (127)
8 AFFY ss66093622 Nov 29, 2006 (127)
9 AFFY ss76050809 Dec 08, 2007 (130)
10 HGSV ss79822589 Dec 15, 2007 (130)
11 KRIBB_YJKIM ss82292778 Dec 16, 2007 (130)
12 HGSV ss83154075 Dec 15, 2007 (130)
13 HGSV ss85321887 Dec 15, 2007 (130)
14 HGSV ss85464937 Dec 15, 2007 (130)
15 BCMHGSC_JDW ss87174402 Mar 23, 2008 (129)
16 HUMANGENOME_JCVI ss97915488 Feb 05, 2009 (130)
17 BGI ss105114935 Dec 01, 2009 (131)
18 1000GENOMES ss107949039 Jan 22, 2009 (130)
19 1000GENOMES ss109967489 Jan 24, 2009 (130)
20 ILLUMINA-UK ss118453511 Feb 14, 2009 (130)
21 ENSEMBL ss131785240 Dec 01, 2009 (131)
22 ENSEMBL ss137763582 Dec 01, 2009 (131)
23 COMPLETE_GENOMICS ss163004859 Jul 04, 2010 (132)
24 COMPLETE_GENOMICS ss163738121 Jul 04, 2010 (132)
25 AFFY ss172324899 Jul 04, 2010 (132)
26 BUSHMAN ss197925071 Jul 04, 2010 (132)
27 BCM-HGSC-SUB ss205099120 Jul 04, 2010 (132)
28 1000GENOMES ss218203275 Jul 14, 2010 (132)
29 1000GENOMES ss230404159 Jul 14, 2010 (132)
30 1000GENOMES ss238123041 Jul 15, 2010 (132)
31 BL ss252880415 May 09, 2011 (134)
32 GMI ss275691460 May 04, 2012 (137)
33 GMI ss283991016 Apr 25, 2013 (138)
34 PJP ss290498323 May 09, 2011 (134)
35 CLINSEQ_SNP ss491582940 May 04, 2012 (137)
36 TISHKOFF ss553734707 Apr 25, 2013 (138)
37 SSMP ss647536492 Apr 25, 2013 (138)
38 EVA-GONL ss974796488 Aug 21, 2014 (142)
39 JMKIDD_LAB ss1067627321 Aug 21, 2014 (142)
40 1000GENOMES ss1289451805 Aug 21, 2014 (142)
41 DDI ss1425693019 Apr 01, 2015 (144)
42 EVA_GENOME_DK ss1573860154 Apr 01, 2015 (144)
43 EVA_UK10K_ALSPAC ss1599427423 Apr 01, 2015 (144)
44 EVA_UK10K_TWINSUK ss1642421456 Apr 01, 2015 (144)
45 EVA_EXAC ss1685262861 Apr 01, 2015 (144)
46 EVA_MGP ss1710885665 Apr 01, 2015 (144)
47 EVA_SVP ss1712306777 Apr 01, 2015 (144)
48 HAMMER_LAB ss1793785137 Sep 08, 2015 (146)
49 WEILL_CORNELL_DGM ss1917992025 Feb 12, 2016 (147)
50 GENOMED ss1966671384 Jul 19, 2016 (147)
51 JJLAB ss2019512163 Sep 14, 2016 (149)
52 USC_VALOUEV ss2147502544 Dec 20, 2016 (150)
53 HUMAN_LONGEVITY ss2159574892 Dec 20, 2016 (150)
54 TOPMED ss2321729844 Dec 20, 2016 (150)
55 SYSTEMSBIOZJU ss2624271839 Nov 08, 2017 (151)
56 GRF ss2697396575 Nov 08, 2017 (151)
57 GNOMAD ss2731058402 Nov 08, 2017 (151)
58 GNOMAD ss2746195662 Nov 08, 2017 (151)
59 GNOMAD ss2750972654 Nov 08, 2017 (151)
60 SWEGEN ss2986201375 Nov 08, 2017 (151)
61 BIOINF_KMB_FNS_UNIBA ss3023519702 Nov 08, 2017 (151)
62 TOPMED ss3067127299 Nov 08, 2017 (151)
63 CSHL ss3343288965 Nov 08, 2017 (151)
64 OMUKHERJEE_ADBS ss3646220211 Oct 11, 2018 (152)
65 URBANLAB ss3646586762 Oct 11, 2018 (152)
66 EGCUT_WGS ss3654302598 Jul 12, 2019 (153)
67 EVA_DECODE ss3686047270 Jul 12, 2019 (153)
68 ACPOP ss3726740072 Jul 12, 2019 (153)
69 EVA ss3745755375 Jul 12, 2019 (153)
70 PACBIO ss3783308795 Jul 12, 2019 (153)
71 PACBIO ss3788985676 Jul 12, 2019 (153)
72 PACBIO ss3793858306 Jul 12, 2019 (153)
73 KHV_HUMAN_GENOMES ss3798777055 Jul 12, 2019 (153)
74 EVA ss3825551292 Apr 25, 2020 (154)
75 EVA ss3825993991 Apr 25, 2020 (154)
76 EVA ss3836384173 Apr 25, 2020 (154)
77 EVA ss3841788337 Apr 25, 2020 (154)
78 SGDP_PRJ ss3848069596 Apr 25, 2020 (154)
79 KRGDB ss3892931174 Apr 25, 2020 (154)
80 FSA-LAB ss3983913132 Apr 25, 2021 (155)
81 FSA-LAB ss3983913133 Apr 25, 2021 (155)
82 EVA ss3986095368 Apr 25, 2021 (155)
83 TOPMED ss4437306427 Apr 25, 2021 (155)
84 TOMMO_GENOMICS ss5142201828 Apr 25, 2021 (155)
85 EVA ss5237158800 Apr 25, 2021 (155)
86 1000Genomes NC_000001.10 - 3732782 Oct 11, 2018 (152)
87 The Avon Longitudinal Study of Parents and Children NC_000001.10 - 3732782 Oct 11, 2018 (152)
88 Genetic variation in the Estonian population NC_000001.10 - 3732782 Oct 11, 2018 (152)
89 ExAC NC_000001.10 - 3732782 Oct 11, 2018 (152)
90 The Danish reference pan genome NC_000001.10 - 3732782 Apr 25, 2020 (154)
91 gnomAD - Genomes NC_000001.11 - 3816218 Apr 25, 2021 (155)
92 gnomAD - Exomes NC_000001.10 - 3732782 Jul 12, 2019 (153)
93 Genome of the Netherlands Release 5 NC_000001.10 - 3732782 Apr 25, 2020 (154)
94 HapMap NC_000001.11 - 3816218 Apr 25, 2020 (154)
95 KOREAN population from KRGDB NC_000001.10 - 3732782 Apr 25, 2020 (154)
96 Medical Genome Project healthy controls from Spanish population NC_000001.10 - 3732782 Apr 25, 2020 (154)
97 Northern Sweden NC_000001.10 - 3732782 Jul 12, 2019 (153)
98 Qatari NC_000001.10 - 3732782 Apr 25, 2020 (154)
99 SGDP_PRJ NC_000001.10 - 3732782 Apr 25, 2020 (154)
100 Siberian NC_000001.10 - 3732782 Apr 25, 2020 (154)
101 8.3KJPN NC_000001.10 - 3732782 Apr 25, 2021 (155)
102 TopMed NC_000001.11 - 3816218 Apr 25, 2021 (155)
103 UK 10K study - Twins NC_000001.10 - 3732782 Oct 11, 2018 (152)
104 A Vietnamese Genetic Variation Database NC_000001.10 - 3732782 Jul 12, 2019 (153)
105 ALFA NC_000001.11 - 3816218 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)
rs17403194 Oct 07, 2004 (123)
rs56612060 May 25, 2008 (130)
rs59301053 May 25, 2008 (130)
rs61701685 Feb 27, 2009 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
108568, ss3892931174 NC_000001.10:3732781:T:A NC_000001.11:3816217:T:A (self)
ss79822589, ss83154075, ss85321887, ss85464937 NC_000001.8:3755938:T:C NC_000001.11:3816217:T:C (self)
ss87174402, ss107949039, ss109967489, ss118453511, ss163004859, ss163738121, ss197925071, ss205099120, ss252880415, ss275691460, ss283991016, ss290498323, ss491582940, ss1712306777 NC_000001.9:3722641:T:C NC_000001.11:3816217:T:C (self)
119836, 53668, 40846, 4439239, 1367388, 73387, 23094, 108568, 2417, 24937, 33955, 86576, 18898, 171135, 53668, 11343, ss218203275, ss230404159, ss238123041, ss553734707, ss647536492, ss974796488, ss1067627321, ss1289451805, ss1425693019, ss1573860154, ss1599427423, ss1642421456, ss1685262861, ss1710885665, ss1793785137, ss1917992025, ss1966671384, ss2019512163, ss2147502544, ss2321729844, ss2624271839, ss2697396575, ss2731058402, ss2746195662, ss2750972654, ss2986201375, ss3343288965, ss3646220211, ss3654302598, ss3726740072, ss3745755375, ss3783308795, ss3788985676, ss3793858306, ss3825551292, ss3825993991, ss3836384173, ss3848069596, ss3892931174, ss3983913132, ss3983913133, ss3986095368, ss5142201828 NC_000001.10:3732781:T:C NC_000001.11:3816217:T:C (self)
864369, 2811, 568244, 912762, 10003382764, ss2159574892, ss3023519702, ss3067127299, ss3646586762, ss3686047270, ss3798777055, ss3841788337, ss4437306427, ss5237158800 NC_000001.11:3816217:T:C NC_000001.11:3816217:T:C (self)
ss9903675, ss12992573, ss19851002, ss20601694 NT_004321.15:1039555:T:C NC_000001.11:3816217:T:C (self)
ss61706815 NT_004321.16:1039556:T:C NC_000001.11:3816217:T:C (self)
ss24243551, ss44124923, ss66093622, ss76050809, ss82292778, ss97915488, ss105114935, ss131785240, ss137763582, ss172324899 NT_004350.19:3211413:T:C NC_000001.11:3816217:T:C (self)
108568, ss3892931174 NC_000001.10:3732781:T:G NC_000001.11:3816217: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 rs6703035

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