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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.

rs7077335

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr10:6273831 (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
C>A / C>T
Variation Type
SNV Single Nucleotide Variation
Frequency
C=0.031847 (8918/280028, ALFA)
C=0.180732 (47838/264690, TOPMED)
C=0.167040 (23402/140098, GnomAD) (+ 20 more)
C=0.27409 (21570/78696, PAGE_STUDY)
C=0.21372 (3582/16760, 8.3KJPN)
C=0.1997 (1000/5008, 1000G)
C=0.0098 (44/4480, Estonian)
C=0.0101 (39/3854, ALSPAC)
C=0.0143 (53/3708, TWINSUK)
C=0.2024 (593/2930, KOREAN)
C=0.1286 (268/2084, HGDP_Stanford)
C=0.2599 (486/1870, HapMap)
C=0.2041 (374/1832, Korea1K)
C=0.014 (14/998, GoNL)
C=0.196 (153/782, PRJEB37584)
C=0.152 (95/626, Chileans)
C=0.003 (2/600, NorthernSweden)
C=0.063 (33/520, SGDP_PRJ)
C=0.060 (13/216, Qatari)
C=0.135 (28/208, Vietnamese)
C=0.00 (0/66, Ancient Sardinia)
C=0.02 (1/56, Siberian)
C=0.03 (1/40, 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 10 NC_000010.11:g.6273831C>A
GRCh38.p13 chr 10 NC_000010.11:g.6273831C>T
GRCh37.p13 chr 10 NC_000010.10:g.6315794C>A
GRCh37.p13 chr 10 NC_000010.10:g.6315794C>T
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 280028 C=0.031847 A=0.968153, T=0.000000
European Sub 247712 C=0.013956 A=0.986044, T=0.000000
African Sub 6006 C=0.5346 A=0.4654, T=0.0000
African Others Sub 242 C=0.653 A=0.347, T=0.000
African American Sub 5764 C=0.5297 A=0.4703, T=0.0000
Asian Sub 3828 C=0.1907 A=0.8093, T=0.0000
East Asian Sub 3106 C=0.2090 A=0.7910, T=0.0000
Other Asian Sub 722 C=0.112 A=0.888, T=0.000
Latin American 1 Sub 1020 C=0.0971 A=0.9029, T=0.0000
Latin American 2 Sub 7696 C=0.0968 A=0.9032, T=0.0000
South Asian Sub 5130 C=0.0090 A=0.9910, T=0.0000
Other Sub 8636 C=0.0730 A=0.9270, T=0.0000


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 C=0.180732 A=0.819268
gnomAD - Genomes Global Study-wide 140098 C=0.167040 A=0.832960
gnomAD - Genomes European Sub 75958 C=0.01164 A=0.98836
gnomAD - Genomes African Sub 41906 C=0.48260 A=0.51740
gnomAD - Genomes American Sub 13636 C=0.09453 A=0.90547
gnomAD - Genomes Ashkenazi Jewish Sub 3324 C=0.0394 A=0.9606
gnomAD - Genomes East Asian Sub 3124 C=0.1882 A=0.8118
gnomAD - Genomes Other Sub 2150 C=0.1330 A=0.8670
The PAGE Study Global Study-wide 78696 C=0.27409 A=0.72591
The PAGE Study AfricanAmerican Sub 32512 C=0.47038 A=0.52962
The PAGE Study Mexican Sub 10810 C=0.09630 A=0.90370
The PAGE Study Asian Sub 8316 C=0.2161 A=0.7839
The PAGE Study PuertoRican Sub 7918 C=0.1444 A=0.8556
The PAGE Study NativeHawaiian Sub 4534 C=0.0690 A=0.9310
The PAGE Study Cuban Sub 4230 C=0.0948 A=0.9052
The PAGE Study Dominican Sub 3828 C=0.2497 A=0.7503
The PAGE Study CentralAmerican Sub 2450 C=0.1233 A=0.8767
The PAGE Study SouthAmerican Sub 1982 C=0.0999 A=0.9001
The PAGE Study NativeAmerican Sub 1260 C=0.0921 A=0.9079
The PAGE Study SouthAsian Sub 856 C=0.012 A=0.988
8.3KJPN JAPANESE Study-wide 16760 C=0.21372 A=0.78628
1000Genomes Global Study-wide 5008 C=0.1997 A=0.8003
1000Genomes African Sub 1322 C=0.5787 A=0.4213
1000Genomes East Asian Sub 1008 C=0.1508 A=0.8492
1000Genomes Europe Sub 1006 C=0.0149 A=0.9851
1000Genomes South Asian Sub 978 C=0.010 A=0.990
1000Genomes American Sub 694 C=0.084 A=0.916
Genetic variation in the Estonian population Estonian Study-wide 4480 C=0.0098 A=0.9902
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 C=0.0101 A=0.9899
UK 10K study - Twins TWIN COHORT Study-wide 3708 C=0.0143 A=0.9857
KOREAN population from KRGDB KOREAN Study-wide 2930 C=0.2024 A=0.7976
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 C=0.1286 A=0.8714
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 C=0.166 A=0.834
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 C=0.022 A=0.978
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 C=0.057 A=0.943
HGDP-CEPH-db Supplement 1 Europe Sub 320 C=0.003 A=0.997
HGDP-CEPH-db Supplement 1 Africa Sub 242 C=0.533 A=0.467
HGDP-CEPH-db Supplement 1 America Sub 216 C=0.125 A=0.875
HGDP-CEPH-db Supplement 1 Oceania Sub 72 C=0.06 A=0.94
HapMap Global Study-wide 1870 C=0.2599 A=0.7401
HapMap American Sub 760 C=0.116 A=0.884
HapMap African Sub 680 C=0.513 A=0.487
HapMap Asian Sub 254 C=0.189 A=0.811
HapMap Europe Sub 176 C=0.006 A=0.994
Korean Genome Project KOREAN Study-wide 1832 C=0.2041 A=0.7959
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 C=0.014 A=0.986
CNV burdens in cranial meningiomas Global Study-wide 782 C=0.196 A=0.804
CNV burdens in cranial meningiomas CRM Sub 782 C=0.196 A=0.804
Chileans Chilean Study-wide 626 C=0.152 A=0.848
Northern Sweden ACPOP Study-wide 600 C=0.003 A=0.997
SGDP_PRJ Global Study-wide 520 C=0.063 A=0.937
Qatari Global Study-wide 216 C=0.060 A=0.940
A Vietnamese Genetic Variation Database Global Study-wide 208 C=0.135 A=0.865
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 66 C=0.00 A=1.00
Siberian Global Study-wide 56 C=0.02 A=0.98
The Danish reference pan genome Danish Study-wide 40 C=0.03 A=0.97
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 C= A T
GRCh38.p13 chr 10 NC_000010.11:g.6273831= NC_000010.11:g.6273831C>A NC_000010.11:g.6273831C>T
GRCh37.p13 chr 10 NC_000010.10:g.6315794= NC_000010.10:g.6315794C>A NC_000010.10:g.6315794C>T
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#.

123 SubSNP, 23 Frequency submissions
No Submitter Submission ID Date (Build)
1 BCM_SSAHASNP ss10599591 Jul 11, 2003 (116)
2 SC_SNP ss16093936 Feb 27, 2004 (120)
3 SSAHASNP ss20684112 Apr 05, 2004 (121)
4 ABI ss39841396 Mar 14, 2006 (126)
5 ILLUMINA ss67537114 Nov 30, 2006 (127)
6 ILLUMINA ss67908298 Nov 30, 2006 (127)
7 ILLUMINA ss68268473 Dec 12, 2006 (127)
8 ILLUMINA ss70906415 May 24, 2008 (130)
9 ILLUMINA ss71503008 May 17, 2007 (127)
10 ILLUMINA ss75743381 Dec 06, 2007 (129)
11 AFFY ss76831657 Dec 08, 2007 (130)
12 HGSV ss78087726 Dec 06, 2007 (129)
13 KRIBB_YJKIM ss84609399 Dec 14, 2007 (130)
14 BCMHGSC_JDW ss88080946 Mar 23, 2008 (129)
15 HUMANGENOME_JCVI ss97532701 Feb 04, 2009 (130)
16 BGI ss102850388 Dec 01, 2009 (131)
17 1000GENOMES ss109197474 Jan 23, 2009 (130)
18 ILLUMINA-UK ss119003934 Dec 01, 2009 (131)
19 ENSEMBL ss131661856 Dec 01, 2009 (131)
20 ENSEMBL ss137961487 Dec 01, 2009 (131)
21 ILLUMINA ss154402445 Dec 01, 2009 (131)
22 GMI ss154522791 Dec 01, 2009 (131)
23 ILLUMINA ss159577715 Dec 01, 2009 (131)
24 ILLUMINA ss160843793 Dec 01, 2009 (131)
25 COMPLETE_GENOMICS ss167743348 Jul 04, 2010 (132)
26 COMPLETE_GENOMICS ss170369401 Jul 04, 2010 (132)
27 ILLUMINA ss174230606 Jul 04, 2010 (132)
28 BUSHMAN ss201097519 Jul 04, 2010 (132)
29 BCM-HGSC-SUB ss207060514 Jul 04, 2010 (132)
30 1000GENOMES ss224544556 Jul 14, 2010 (132)
31 1000GENOMES ss235038092 Jul 15, 2010 (132)
32 1000GENOMES ss241773906 Jul 15, 2010 (132)
33 BL ss254025838 May 09, 2011 (134)
34 GMI ss280464772 May 04, 2012 (137)
35 GMI ss286122487 Apr 25, 2013 (138)
36 PJP ss290900168 May 09, 2011 (134)
37 ILLUMINA ss481453388 May 04, 2012 (137)
38 ILLUMINA ss481481209 May 04, 2012 (137)
39 ILLUMINA ss482460855 Sep 08, 2015 (146)
40 ILLUMINA ss485521850 May 04, 2012 (137)
41 ILLUMINA ss537430763 Sep 08, 2015 (146)
42 TISHKOFF ss561745428 Apr 25, 2013 (138)
43 SSMP ss656251660 Apr 25, 2013 (138)
44 ILLUMINA ss778591114 Sep 08, 2015 (146)
45 ILLUMINA ss783206452 Sep 08, 2015 (146)
46 ILLUMINA ss784161259 Sep 08, 2015 (146)
47 ILLUMINA ss832466503 Sep 08, 2015 (146)
48 ILLUMINA ss833088780 Jul 13, 2019 (153)
49 ILLUMINA ss834048311 Sep 08, 2015 (146)
50 EVA-GONL ss987157345 Aug 21, 2014 (142)
51 JMKIDD_LAB ss1076731736 Aug 21, 2014 (142)
52 1000GENOMES ss1336130249 Aug 21, 2014 (142)
53 DDI ss1426208853 Apr 01, 2015 (144)
54 EVA_GENOME_DK ss1574889263 Apr 01, 2015 (144)
55 EVA_DECODE ss1596805313 Apr 01, 2015 (144)
56 EVA_UK10K_ALSPAC ss1623911834 Apr 01, 2015 (144)
57 EVA_UK10K_TWINSUK ss1666905867 Apr 01, 2015 (144)
58 EVA_SVP ss1713154112 Apr 01, 2015 (144)
59 ILLUMINA ss1751975117 Sep 08, 2015 (146)
60 HAMMER_LAB ss1806238314 Sep 08, 2015 (146)
61 WEILL_CORNELL_DGM ss1930478273 Feb 12, 2016 (147)
62 ILLUMINA ss1946275122 Feb 12, 2016 (147)
63 ILLUMINA ss1959236927 Feb 12, 2016 (147)
64 GENOMED ss1967049561 Jul 19, 2016 (147)
65 JJLAB ss2025962275 Sep 14, 2016 (149)
66 USC_VALOUEV ss2154204310 Dec 20, 2016 (150)
67 HUMAN_LONGEVITY ss2172358757 Dec 20, 2016 (150)
68 TOPMED ss2335067854 Dec 20, 2016 (150)
69 SYSTEMSBIOZJU ss2627450043 Nov 08, 2017 (151)
70 ILLUMINA ss2632669816 Nov 08, 2017 (151)
71 GRF ss2698428221 Nov 08, 2017 (151)
72 ILLUMINA ss2710701789 Nov 08, 2017 (151)
73 GNOMAD ss2885105553 Nov 08, 2017 (151)
74 AFFY ss2985550202 Nov 08, 2017 (151)
75 SWEGEN ss3005875671 Nov 08, 2017 (151)
76 ILLUMINA ss3021210828 Nov 08, 2017 (151)
77 BIOINF_KMB_FNS_UNIBA ss3026764651 Nov 08, 2017 (151)
78 TOPMED ss3110664842 Nov 08, 2017 (151)
79 TOPMED ss3110664843 Nov 08, 2017 (151)
80 CSHL ss3348941958 Nov 08, 2017 (151)
81 ILLUMINA ss3625572929 Oct 12, 2018 (152)
82 ILLUMINA ss3630697723 Oct 12, 2018 (152)
83 ILLUMINA ss3632937000 Oct 12, 2018 (152)
84 ILLUMINA ss3633633618 Oct 12, 2018 (152)
85 ILLUMINA ss3634388407 Oct 12, 2018 (152)
86 ILLUMINA ss3635326453 Oct 12, 2018 (152)
87 ILLUMINA ss3636068224 Oct 12, 2018 (152)
88 ILLUMINA ss3637077039 Oct 12, 2018 (152)
89 ILLUMINA ss3637831851 Oct 12, 2018 (152)
90 ILLUMINA ss3638931206 Oct 12, 2018 (152)
91 ILLUMINA ss3639777143 Oct 12, 2018 (152)
92 ILLUMINA ss3640095755 Oct 12, 2018 (152)
93 ILLUMINA ss3640996893 Oct 12, 2018 (152)
94 ILLUMINA ss3641291094 Oct 12, 2018 (152)
95 ILLUMINA ss3642836746 Oct 12, 2018 (152)
96 ILLUMINA ss3643830101 Oct 12, 2018 (152)
97 ILLUMINA ss3644527795 Oct 12, 2018 (152)
98 URBANLAB ss3649280465 Oct 12, 2018 (152)
99 ILLUMINA ss3651558731 Oct 12, 2018 (152)
100 EGCUT_WGS ss3673402793 Jul 13, 2019 (153)
101 EVA_DECODE ss3689206630 Jul 13, 2019 (153)
102 ILLUMINA ss3725132332 Jul 13, 2019 (153)
103 ACPOP ss3737026955 Jul 13, 2019 (153)
104 ILLUMINA ss3744065520 Jul 13, 2019 (153)
105 ILLUMINA ss3744689281 Jul 13, 2019 (153)
106 EVA ss3747699712 Jul 13, 2019 (153)
107 PAGE_CC ss3771539516 Jul 13, 2019 (153)
108 ILLUMINA ss3772189994 Jul 13, 2019 (153)
109 PACBIO ss3786570211 Jul 13, 2019 (153)
110 PACBIO ss3791764099 Jul 13, 2019 (153)
111 PACBIO ss3796645879 Jul 13, 2019 (153)
112 KHV_HUMAN_GENOMES ss3813062673 Jul 13, 2019 (153)
113 EVA ss3831947044 Apr 26, 2020 (154)
114 EVA ss3839504358 Apr 26, 2020 (154)
115 EVA ss3844970340 Apr 26, 2020 (154)
116 HGDP ss3847374087 Apr 26, 2020 (154)
117 SGDP_PRJ ss3873453554 Apr 26, 2020 (154)
118 KRGDB ss3921389027 Apr 26, 2020 (154)
119 KOGIC ss3967131426 Apr 26, 2020 (154)
120 EVA ss3984629133 Apr 26, 2021 (155)
121 EVA ss3985455318 Apr 26, 2021 (155)
122 TOPMED ss4841244008 Apr 26, 2021 (155)
123 TOMMO_GENOMICS ss5196096982 Apr 26, 2021 (155)
124 1000Genomes NC_000010.10 - 6315794 Oct 12, 2018 (152)
125 The Avon Longitudinal Study of Parents and Children NC_000010.10 - 6315794 Oct 12, 2018 (152)
126 Chileans NC_000010.10 - 6315794 Apr 26, 2020 (154)
127 Genetic variation in the Estonian population NC_000010.10 - 6315794 Oct 12, 2018 (152)
128 The Danish reference pan genome NC_000010.10 - 6315794 Apr 26, 2020 (154)
129 gnomAD - Genomes NC_000010.11 - 6273831 Apr 26, 2021 (155)
130 Genome of the Netherlands Release 5 NC_000010.10 - 6315794 Apr 26, 2020 (154)
131 HGDP-CEPH-db Supplement 1 NC_000010.9 - 6355800 Apr 26, 2020 (154)
132 HapMap NC_000010.11 - 6273831 Apr 26, 2020 (154)
133 KOREAN population from KRGDB NC_000010.10 - 6315794 Apr 26, 2020 (154)
134 Korean Genome Project NC_000010.11 - 6273831 Apr 26, 2020 (154)
135 Northern Sweden NC_000010.10 - 6315794 Jul 13, 2019 (153)
136 The PAGE Study NC_000010.11 - 6273831 Jul 13, 2019 (153)
137 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000010.10 - 6315794 Apr 26, 2021 (155)
138 CNV burdens in cranial meningiomas NC_000010.10 - 6315794 Apr 26, 2021 (155)
139 Qatari NC_000010.10 - 6315794 Apr 26, 2020 (154)
140 SGDP_PRJ NC_000010.10 - 6315794 Apr 26, 2020 (154)
141 Siberian NC_000010.10 - 6315794 Apr 26, 2020 (154)
142 8.3KJPN NC_000010.10 - 6315794 Apr 26, 2021 (155)
143 TopMed NC_000010.11 - 6273831 Apr 26, 2021 (155)
144 UK 10K study - Twins NC_000010.10 - 6315794 Oct 12, 2018 (152)
145 A Vietnamese Genetic Variation Database NC_000010.10 - 6315794 Jul 13, 2019 (153)
146 ALFA NC_000010.11 - 6273831 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)
rs56444078 May 24, 2008 (130)
rs57792801 May 24, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss78087726, ss3638931206, ss3639777143, ss3643830101 NC_000010.8:6355799:C:A NC_000010.11:6273830:C:A (self)
51979, ss88080946, ss109197474, ss119003934, ss167743348, ss170369401, ss201097519, ss207060514, ss254025838, ss280464772, ss286122487, ss290900168, ss481453388, ss1596805313, ss1713154112, ss3642836746, ss3847374087 NC_000010.9:6355799:C:A NC_000010.11:6273830:C:A (self)
48471566, 26932243, 41158, 19141041, 2014466, 12012229, 28566421, 10311820, 681245, 178589, 12520203, 25470534, 6720664, 54066289, 26932243, 5978605, ss224544556, ss235038092, ss241773906, ss481481209, ss482460855, ss485521850, ss537430763, ss561745428, ss656251660, ss778591114, ss783206452, ss784161259, ss832466503, ss833088780, ss834048311, ss987157345, ss1076731736, ss1336130249, ss1426208853, ss1574889263, ss1623911834, ss1666905867, ss1751975117, ss1806238314, ss1930478273, ss1946275122, ss1959236927, ss1967049561, ss2025962275, ss2154204310, ss2335067854, ss2627450043, ss2632669816, ss2698428221, ss2710701789, ss2885105553, ss2985550202, ss3005875671, ss3021210828, ss3348941958, ss3625572929, ss3630697723, ss3632937000, ss3633633618, ss3634388407, ss3635326453, ss3636068224, ss3637077039, ss3637831851, ss3640095755, ss3640996893, ss3641291094, ss3644527795, ss3651558731, ss3673402793, ss3737026955, ss3744065520, ss3744689281, ss3747699712, ss3772189994, ss3786570211, ss3791764099, ss3796645879, ss3831947044, ss3839504358, ss3873453554, ss3921389027, ss3984629133, ss3985455318, ss5196096982 NC_000010.10:6315793:C:A NC_000010.11:6273830:C:A (self)
342416716, 330077, 23509427, 760985, 35684453, 56789663, 2996698775, ss2172358757, ss3026764651, ss3110664842, ss3649280465, ss3689206630, ss3725132332, ss3771539516, ss3813062673, ss3844970340, ss3967131426, ss4841244008 NC_000010.11:6273830:C:A NC_000010.11:6273830:C:A (self)
ss39841396, ss67537114, ss67908298, ss68268473, ss70906415, ss71503008, ss75743381, ss76831657, ss84609399, ss97532701, ss102850388, ss131661856, ss137961487, ss154402445, ss154522791, ss159577715, ss160843793, ss174230606 NT_008705.16:6255793:C:A NC_000010.11:6273830:C:A (self)
ss10599591, ss16093936, ss20684112 NT_077569.2:678689:C:A NC_000010.11:6273830:C:A (self)
2996698775, ss3110664843 NC_000010.11:6273830:C:T NC_000010.11:6273830:C: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 rs7077335

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