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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.

rs671164

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr18:42932170 (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
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.195417 (51725/264690, TOPMED)
A=0.115415 (29011/251362, ALFA)
A=0.177188 (24813/140038, GnomAD) (+ 21 more)
A=0.28098 (22111/78692, PAGE_STUDY)
A=0.48439 (13688/28258, 14KJPN)
A=0.48204 (8079/16760, 8.3KJPN)
A=0.2388 (1529/6404, 1000G_30x)
A=0.2412 (1208/5008, 1000G)
A=0.1165 (522/4480, Estonian)
A=0.1048 (404/3854, ALSPAC)
A=0.0957 (355/3708, TWINSUK)
A=0.4212 (1234/2930, KOREAN)
A=0.2260 (471/2084, HGDP_Stanford)
A=0.2598 (491/1890, HapMap)
A=0.4465 (818/1832, Korea1K)
A=0.091 (91/998, GoNL)
A=0.335 (259/772, PRJEB37584)
A=0.082 (49/600, NorthernSweden)
A=0.199 (43/216, Qatari)
A=0.259 (55/212, Vietnamese)
G=0.407 (83/204, SGDP_PRJ)
A=0.07 (4/58, Ancient Sardinia)
A=0.07 (3/40, GENOME_DK)
G=0.45 (10/22, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
RIT2 : 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 256398 G=0.883794 A=0.116206
European Sub 226534 G=0.902284 A=0.097716
African Sub 8684 G=0.7336 A=0.2664
African Others Sub 350 G=0.711 A=0.289
African American Sub 8334 G=0.7346 A=0.2654
Asian Sub 3866 G=0.6433 A=0.3567
East Asian Sub 3134 G=0.6008 A=0.3992
Other Asian Sub 732 G=0.825 A=0.175
Latin American 1 Sub 1042 G=0.8292 A=0.1708
Latin American 2 Sub 6650 G=0.6632 A=0.3368
South Asian Sub 366 G=0.833 A=0.167
Other Sub 9256 G=0.8392 A=0.1608


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=0.804583 A=0.195417
Allele Frequency Aggregator Total Global 251362 G=0.884585 A=0.115415
Allele Frequency Aggregator European Sub 223440 G=0.902363 A=0.097637
Allele Frequency Aggregator Other Sub 8456 G=0.8456 A=0.1544
Allele Frequency Aggregator African Sub 7542 G=0.7307 A=0.2693
Allele Frequency Aggregator Latin American 2 Sub 6650 G=0.6632 A=0.3368
Allele Frequency Aggregator Asian Sub 3866 G=0.6433 A=0.3567
Allele Frequency Aggregator Latin American 1 Sub 1042 G=0.8292 A=0.1708
Allele Frequency Aggregator South Asian Sub 366 G=0.833 A=0.167
gnomAD - Genomes Global Study-wide 140038 G=0.822812 A=0.177188
gnomAD - Genomes European Sub 75894 G=0.89315 A=0.10685
gnomAD - Genomes African Sub 41956 G=0.73086 A=0.26914
gnomAD - Genomes American Sub 13616 G=0.73392 A=0.26608
gnomAD - Genomes Ashkenazi Jewish Sub 3320 G=0.8741 A=0.1259
gnomAD - Genomes East Asian Sub 3104 G=0.6765 A=0.3235
gnomAD - Genomes Other Sub 2148 G=0.8291 A=0.1709
The PAGE Study Global Study-wide 78692 G=0.71902 A=0.28098
The PAGE Study AfricanAmerican Sub 32514 G=0.73642 A=0.26358
The PAGE Study Mexican Sub 10808 G=0.65997 A=0.34003
The PAGE Study Asian Sub 8318 G=0.5464 A=0.4536
The PAGE Study PuertoRican Sub 7916 G=0.7873 A=0.2127
The PAGE Study NativeHawaiian Sub 4534 G=0.7640 A=0.2360
The PAGE Study Cuban Sub 4226 G=0.8516 A=0.1484
The PAGE Study Dominican Sub 3828 G=0.7853 A=0.2147
The PAGE Study CentralAmerican Sub 2450 G=0.6784 A=0.3216
The PAGE Study SouthAmerican Sub 1982 G=0.6504 A=0.3496
The PAGE Study NativeAmerican Sub 1260 G=0.7976 A=0.2024
The PAGE Study SouthAsian Sub 856 G=0.820 A=0.180
14KJPN JAPANESE Study-wide 28258 G=0.51561 A=0.48439
8.3KJPN JAPANESE Study-wide 16760 G=0.51796 A=0.48204
1000Genomes_30x Global Study-wide 6404 G=0.7612 A=0.2388
1000Genomes_30x African Sub 1786 G=0.6993 A=0.3007
1000Genomes_30x Europe Sub 1266 G=0.9076 A=0.0924
1000Genomes_30x South Asian Sub 1202 G=0.8428 A=0.1572
1000Genomes_30x East Asian Sub 1170 G=0.6479 A=0.3521
1000Genomes_30x American Sub 980 G=0.720 A=0.280
1000Genomes Global Study-wide 5008 G=0.7588 A=0.2412
1000Genomes African Sub 1322 G=0.6936 A=0.3064
1000Genomes East Asian Sub 1008 G=0.6448 A=0.3552
1000Genomes Europe Sub 1006 G=0.9056 A=0.0944
1000Genomes South Asian Sub 978 G=0.843 A=0.157
1000Genomes American Sub 694 G=0.718 A=0.282
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.8835 A=0.1165
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.8952 A=0.1048
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.9043 A=0.0957
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.5788 A=0.4212
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 G=0.7740 A=0.2260
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 G=0.681 A=0.319
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 G=0.819 A=0.181
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 G=0.851 A=0.149
HGDP-CEPH-db Supplement 1 Europe Sub 320 G=0.919 A=0.081
HGDP-CEPH-db Supplement 1 Africa Sub 242 G=0.756 A=0.244
HGDP-CEPH-db Supplement 1 America Sub 216 G=0.505 A=0.495
HGDP-CEPH-db Supplement 1 Oceania Sub 72 G=0.97 A=0.03
HapMap Global Study-wide 1890 G=0.7402 A=0.2598
HapMap American Sub 770 G=0.818 A=0.182
HapMap African Sub 690 G=0.670 A=0.330
HapMap Asian Sub 254 G=0.563 A=0.437
HapMap Europe Sub 176 G=0.932 A=0.068
Korean Genome Project KOREAN Study-wide 1832 G=0.5535 A=0.4465
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.909 A=0.091
CNV burdens in cranial meningiomas Global Study-wide 772 G=0.665 A=0.335
CNV burdens in cranial meningiomas CRM Sub 772 G=0.665 A=0.335
Northern Sweden ACPOP Study-wide 600 G=0.918 A=0.082
Qatari Global Study-wide 216 G=0.801 A=0.199
A Vietnamese Genetic Variation Database Global Study-wide 212 G=0.741 A=0.259
SGDP_PRJ Global Study-wide 204 G=0.407 A=0.593
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 58 G=0.93 A=0.07
The Danish reference pan genome Danish Study-wide 40 G=0.93 A=0.07
Siberian Global Study-wide 22 G=0.45 A=0.55
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 18 NC_000018.10:g.42932170G>A
GRCh37.p13 chr 18 NC_000018.9:g.40512135G>A
Gene: RIT2, Ras like without CAAX 2 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
RIT2 transcript variant 2 NM_001272077.2:c.235-8407…

NM_001272077.2:c.235-8407C>T

 		N/A Intron Variant
RIT2 transcript variant 1 NM_002930.4:c.235-8407C>T 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 G= A
GRCh38.p14 chr 18 NC_000018.10:g.42932170= NC_000018.10:g.42932170G>A
GRCh37.p13 chr 18 NC_000018.9:g.40512135= NC_000018.9:g.40512135G>A
RIT2 transcript variant 2 NM_001272077.1:c.235-8407= NM_001272077.1:c.235-8407C>T
RIT2 transcript variant 2 NM_001272077.2:c.235-8407= NM_001272077.2:c.235-8407C>T
RIT2 transcript variant 1 NM_002930.3:c.235-8407= NM_002930.3:c.235-8407C>T
RIT2 transcript variant 1 NM_002930.4:c.235-8407= NM_002930.4:c.235-8407C>T
RIT2 transcript variant X1 XM_005258327.1:c.178-8407= XM_005258327.1:c.178-8407C>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#.

116 SubSNP, 24 Frequency submissions
No Submitter Submission ID Date (Build)
1 SC_JCM ss844550 Aug 11, 2000 (83)
2 SC_JCM ss2435119 Nov 09, 2000 (92)
3 TSC-CSHL ss2837913 Jan 22, 2001 (92)
4 WI_SSAHASNP ss12444030 Jul 11, 2003 (116)
5 ABI ss44141857 Mar 14, 2006 (126)
6 ILLUMINA ss67846569 Nov 29, 2006 (127)
7 ILLUMINA ss71472051 May 16, 2007 (127)
8 ILLUMINA ss75407898 Dec 07, 2007 (129)
9 HGSV ss81699902 Dec 15, 2007 (130)
10 1000GENOMES ss114321322 Jan 25, 2009 (130)
11 ILLUMINA-UK ss117855495 Feb 14, 2009 (130)
12 KRIBB_YJKIM ss119362289 Dec 01, 2009 (131)
13 ILLUMINA ss160800925 Dec 01, 2009 (131)
14 COMPLETE_GENOMICS ss168128402 Jul 04, 2010 (132)
15 COMPLETE_GENOMICS ss169655345 Jul 04, 2010 (132)
16 ILLUMINA ss174079973 Jul 04, 2010 (132)
17 1000GENOMES ss227839778 Jul 14, 2010 (132)
18 1000GENOMES ss237450906 Jul 15, 2010 (132)
19 1000GENOMES ss243703517 Jul 15, 2010 (132)
20 GMI ss282976328 May 04, 2012 (137)
21 GMI ss287276593 Apr 25, 2013 (138)
22 ILLUMINA ss481326745 May 04, 2012 (137)
23 ILLUMINA ss481352011 May 04, 2012 (137)
24 ILLUMINA ss482333055 Sep 08, 2015 (146)
25 ILLUMINA ss485458517 May 04, 2012 (137)
26 ILLUMINA ss537382024 Sep 08, 2015 (146)
27 TISHKOFF ss565618638 Apr 25, 2013 (138)
28 SSMP ss661448669 Apr 25, 2013 (138)
29 ILLUMINA ss778948791 Sep 08, 2015 (146)
30 ILLUMINA ss783174735 Aug 21, 2014 (142)
31 ILLUMINA ss784130179 Sep 08, 2015 (146)
32 ILLUMINA ss832434317 Apr 01, 2015 (144)
33 ILLUMINA ss834410613 Sep 08, 2015 (146)
34 EVA-GONL ss993689939 Aug 21, 2014 (142)
35 JMKIDD_LAB ss1081472537 Aug 21, 2014 (142)
36 1000GENOMES ss1360885074 Aug 21, 2014 (142)
37 EVA_GENOME_DK ss1578387651 Apr 01, 2015 (144)
38 EVA_UK10K_ALSPAC ss1636795336 Apr 01, 2015 (144)
39 EVA_UK10K_TWINSUK ss1679789369 Apr 01, 2015 (144)
40 EVA_DECODE ss1697746447 Apr 01, 2015 (144)
41 EVA_SVP ss1713623081 Apr 01, 2015 (144)
42 ILLUMINA ss1752255806 Sep 08, 2015 (146)
43 WEILL_CORNELL_DGM ss1937158594 Feb 12, 2016 (147)
44 ILLUMINA ss1946499541 Feb 12, 2016 (147)
45 ILLUMINA ss1959801582 Feb 12, 2016 (147)
46 GENOMED ss1968515029 Jul 19, 2016 (147)
47 JJLAB ss2029348497 Sep 14, 2016 (149)
48 ILLUMINA ss2095079991 Dec 20, 2016 (150)
49 USC_VALOUEV ss2157852923 Dec 20, 2016 (150)
50 HUMAN_LONGEVITY ss2221280663 Dec 20, 2016 (150)
51 SYSTEMSBIOZJU ss2629172366 Nov 08, 2017 (151)
52 ILLUMINA ss2633468383 Nov 08, 2017 (151)
53 GRF ss2702438948 Nov 08, 2017 (151)
54 ILLUMINA ss2710867070 Nov 08, 2017 (151)
55 GNOMAD ss2956294588 Nov 08, 2017 (151)
56 SWEGEN ss3016469608 Nov 08, 2017 (151)
57 ILLUMINA ss3021840148 Nov 08, 2017 (151)
58 BIOINF_KMB_FNS_UNIBA ss3028501807 Nov 08, 2017 (151)
59 CSHL ss3352006426 Nov 08, 2017 (151)
60 ILLUMINA ss3625724822 Oct 12, 2018 (152)
61 ILLUMINA ss3627800584 Oct 12, 2018 (152)
62 ILLUMINA ss3631445188 Oct 12, 2018 (152)
63 ILLUMINA ss3633161252 Oct 12, 2018 (152)
64 ILLUMINA ss3633869986 Oct 12, 2018 (152)
65 ILLUMINA ss3634704420 Oct 12, 2018 (152)
66 ILLUMINA ss3635557294 Oct 12, 2018 (152)
67 ILLUMINA ss3636393668 Oct 12, 2018 (152)
68 ILLUMINA ss3637308902 Oct 12, 2018 (152)
69 ILLUMINA ss3638194077 Oct 12, 2018 (152)
70 ILLUMINA ss3640411728 Oct 12, 2018 (152)
71 ILLUMINA ss3641089433 Oct 12, 2018 (152)
72 ILLUMINA ss3641384983 Oct 12, 2018 (152)
73 ILLUMINA ss3643170033 Oct 12, 2018 (152)
74 ILLUMINA ss3644705039 Oct 12, 2018 (152)
75 ILLUMINA ss3652261411 Oct 12, 2018 (152)
76 EGCUT_WGS ss3683308202 Jul 13, 2019 (153)
77 EVA_DECODE ss3701589456 Jul 13, 2019 (153)
78 ILLUMINA ss3725673843 Jul 13, 2019 (153)
79 ACPOP ss3742512475 Jul 13, 2019 (153)
80 ILLUMINA ss3744158219 Jul 13, 2019 (153)
81 ILLUMINA ss3745004568 Jul 13, 2019 (153)
82 EVA ss3755343763 Jul 13, 2019 (153)
83 PAGE_CC ss3771969618 Jul 13, 2019 (153)
84 ILLUMINA ss3772502079 Jul 13, 2019 (153)
85 PACBIO ss3788360793 Jul 13, 2019 (153)
86 PACBIO ss3793293269 Jul 13, 2019 (153)
87 PACBIO ss3798179614 Jul 13, 2019 (153)
88 KHV_HUMAN_GENOMES ss3820608936 Jul 13, 2019 (153)
89 EVA ss3835151289 Apr 27, 2020 (154)
90 HGDP ss3847582065 Apr 27, 2020 (154)
91 SGDP_PRJ ss3886947072 Apr 27, 2020 (154)
92 KRGDB ss3936809109 Apr 27, 2020 (154)
93 KOGIC ss3980083282 Apr 27, 2020 (154)
94 EVA ss3984732248 Apr 27, 2021 (155)
95 EVA ss3985823561 Apr 27, 2021 (155)
96 EVA ss4017796221 Apr 27, 2021 (155)
97 TOPMED ss5055465377 Apr 27, 2021 (155)
98 TOMMO_GENOMICS ss5225014270 Apr 27, 2021 (155)
99 1000G_HIGH_COVERAGE ss5305173089 Oct 16, 2022 (156)
100 EVA ss5315930218 Oct 16, 2022 (156)
101 EVA ss5431198095 Oct 16, 2022 (156)
102 HUGCELL_USP ss5497956117 Oct 16, 2022 (156)
103 EVA ss5511925502 Oct 16, 2022 (156)
104 1000G_HIGH_COVERAGE ss5609952664 Oct 16, 2022 (156)
105 SANFORD_IMAGENETICS ss5624412910 Oct 16, 2022 (156)
106 SANFORD_IMAGENETICS ss5661227135 Oct 16, 2022 (156)
107 TOMMO_GENOMICS ss5782760824 Oct 16, 2022 (156)
108 EVA ss5799992324 Oct 16, 2022 (156)
109 YY_MCH ss5817066172 Oct 16, 2022 (156)
110 EVA ss5827495518 Oct 16, 2022 (156)
111 EVA ss5847485792 Oct 16, 2022 (156)
112 EVA ss5847820332 Oct 16, 2022 (156)
113 EVA ss5852038045 Oct 16, 2022 (156)
114 EVA ss5873941501 Oct 16, 2022 (156)
115 EVA ss5952636696 Oct 16, 2022 (156)
116 EVA ss5979526439 Oct 16, 2022 (156)
117 1000Genomes NC_000018.9 - 40512135 Oct 12, 2018 (152)
118 1000Genomes_30x NC_000018.10 - 42932170 Oct 16, 2022 (156)
119 The Avon Longitudinal Study of Parents and Children NC_000018.9 - 40512135 Oct 12, 2018 (152)
120 Genetic variation in the Estonian population NC_000018.9 - 40512135 Oct 12, 2018 (152)
121 The Danish reference pan genome NC_000018.9 - 40512135 Apr 27, 2020 (154)
122 gnomAD - Genomes NC_000018.10 - 42932170 Apr 27, 2021 (155)
123 Genome of the Netherlands Release 5 NC_000018.9 - 40512135 Apr 27, 2020 (154)
124 HGDP-CEPH-db Supplement 1 NC_000018.8 - 38766133 Apr 27, 2020 (154)
125 HapMap NC_000018.10 - 42932170 Apr 27, 2020 (154)
126 KOREAN population from KRGDB NC_000018.9 - 40512135 Apr 27, 2020 (154)
127 Korean Genome Project NC_000018.10 - 42932170 Apr 27, 2020 (154)
128 Northern Sweden NC_000018.9 - 40512135 Jul 13, 2019 (153)
129 The PAGE Study NC_000018.10 - 42932170 Jul 13, 2019 (153)
130 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000018.9 - 40512135 Apr 27, 2021 (155)
131 CNV burdens in cranial meningiomas NC_000018.9 - 40512135 Apr 27, 2021 (155)
132 Qatari NC_000018.9 - 40512135 Apr 27, 2020 (154)
133 SGDP_PRJ NC_000018.9 - 40512135 Apr 27, 2020 (154)
134 Siberian NC_000018.9 - 40512135 Apr 27, 2020 (154)
135 8.3KJPN NC_000018.9 - 40512135 Apr 27, 2021 (155)
136 14KJPN NC_000018.10 - 42932170 Oct 16, 2022 (156)
137 TopMed NC_000018.10 - 42932170 Apr 27, 2021 (155)
138 UK 10K study - Twins NC_000018.9 - 40512135 Oct 12, 2018 (152)
139 A Vietnamese Genetic Variation Database NC_000018.9 - 40512135 Jul 13, 2019 (153)
140 ALFA NC_000018.10 - 42932170 Apr 27, 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)
rs1619421 Jan 18, 2001 (92)
rs58631883 May 24, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
259957, ss81699902, ss114321322, ss117855495, ss168128402, ss169655345, ss282976328, ss287276593, ss481326745, ss1697746447, ss1713623081, ss3643170033, ss3847582065 NC_000018.8:38766132:G:A NC_000018.10:42932169:G:A (self)
74209645, 41111572, 29046450, 4580337, 18318307, 43986503, 15797340, 1049488, 281800, 19200516, 38964052, 10369277, 82983577, 41111572, 9083993, ss227839778, ss237450906, ss243703517, ss481352011, ss482333055, ss485458517, ss537382024, ss565618638, ss661448669, ss778948791, ss783174735, ss784130179, ss832434317, ss834410613, ss993689939, ss1081472537, ss1360885074, ss1578387651, ss1636795336, ss1679789369, ss1752255806, ss1937158594, ss1946499541, ss1959801582, ss1968515029, ss2029348497, ss2095079991, ss2157852923, ss2629172366, ss2633468383, ss2702438948, ss2710867070, ss2956294588, ss3016469608, ss3021840148, ss3352006426, ss3625724822, ss3627800584, ss3631445188, ss3633161252, ss3633869986, ss3634704420, ss3635557294, ss3636393668, ss3637308902, ss3638194077, ss3640411728, ss3641089433, ss3641384983, ss3644705039, ss3652261411, ss3683308202, ss3742512475, ss3744158219, ss3745004568, ss3755343763, ss3772502079, ss3788360793, ss3793293269, ss3798179614, ss3835151289, ss3886947072, ss3936809109, ss3984732248, ss3985823561, ss4017796221, ss5225014270, ss5315930218, ss5431198095, ss5511925502, ss5624412910, ss5661227135, ss5799992324, ss5827495518, ss5847485792, ss5847820332, ss5952636696, ss5979526439 NC_000018.9:40512134:G:A NC_000018.10:42932169:G:A (self)
97478599, 523532909, 1594552, 36461283, 1191087, 116597928, 271011040, 719146474, ss2221280663, ss3028501807, ss3701589456, ss3725673843, ss3771969618, ss3820608936, ss3980083282, ss5055465377, ss5305173089, ss5497956117, ss5609952664, ss5782760824, ss5817066172, ss5852038045, ss5873941501 NC_000018.10:42932169:G:A NC_000018.10:42932169:G:A (self)
ss12444030 NT_010966.13:22001236:G:A NC_000018.10:42932169:G:A (self)
ss844550, ss2435119, ss2837913, ss44141857, ss67846569, ss71472051, ss75407898, ss119362289, ss160800925, ss174079973 NT_010966.14:22001236:G:A NC_000018.10:42932169:G:A (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 rs671164

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