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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.

rs2657167

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr11:4546105 (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>G
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.424172 (112274/264690, TOPMED)
G=0.429595 (60109/139920, GnomAD)
G=0.41953 (33016/78698, PAGE_STUDY) (+ 20 more)
G=0.40707 (21193/52062, ALFA)
G=0.34622 (5802/16758, 8.3KJPN)
G=0.44430 (5775/12998, GO-ESP)
G=0.4255 (2131/5008, 1000G)
G=0.3685 (1651/4480, Estonian)
G=0.3934 (1516/3854, ALSPAC)
G=0.3927 (1456/3708, TWINSUK)
G=0.3628 (1063/2930, KOREAN)
G=0.4302 (814/1892, HapMap)
G=0.391 (390/998, GoNL)
G=0.371 (289/780, PRJEB37584)
G=0.357 (214/600, NorthernSweden)
G=0.313 (167/534, MGP)
G=0.137 (72/525, Vietnamese)
C=0.376 (124/330, SGDP_PRJ)
G=0.355 (108/304, FINRISK)
G=0.421 (91/216, Qatari)
G=0.32 (26/82, Ancient Sardinia)
G=0.45 (18/40, GENOME_DK)
C=0.39 (15/38, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
OR52M1 : Missense 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 11 NC_000011.10:g.4546105C>A
GRCh38.p13 chr 11 NC_000011.10:g.4546105C>G
GRCh37.p13 chr 11 NC_000011.9:g.4567335C>A
GRCh37.p13 chr 11 NC_000011.9:g.4567335C>G
Gene: OR52M1, olfactory receptor family 52 subfamily M member 1 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
OR52M1 transcript NM_001004137.1:c.915C>A S [AGC] > R [AGA] Coding Sequence Variant
olfactory receptor 52M1 NP_001004137.1:p.Ser305Arg S (Ser) > R (Arg) Missense Variant
OR52M1 transcript NM_001004137.1:c.915C>G S [AGC] > R [AGG] Coding Sequence Variant
olfactory receptor 52M1 NP_001004137.1:p.Ser305Arg S (Ser) > R (Arg) Missense 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 52062 C=0.59293 G=0.40707
European Sub 40100 C=0.60022 G=0.39978
African Sub 3574 C=0.4709 G=0.5291
African Others Sub 122 C=0.393 G=0.607
African American Sub 3452 C=0.4736 G=0.5264
Asian Sub 168 C=0.655 G=0.345
East Asian Sub 112 C=0.652 G=0.348
Other Asian Sub 56 C=0.66 G=0.34
Latin American 1 Sub 500 C=0.536 G=0.464
Latin American 2 Sub 628 C=0.803 G=0.197
South Asian Sub 98 C=0.49 G=0.51
Other Sub 6994 C=0.5987 G=0.4013


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=0.575828 G=0.424172
gnomAD - Genomes Global Study-wide 139920 C=0.570405 G=0.429595
gnomAD - Genomes European Sub 75802 C=0.60592 G=0.39408
gnomAD - Genomes African Sub 41888 C=0.46075 G=0.53925
gnomAD - Genomes American Sub 13642 C=0.69389 G=0.30611
gnomAD - Genomes Ashkenazi Jewish Sub 3322 C=0.5473 G=0.4527
gnomAD - Genomes East Asian Sub 3120 C=0.6529 G=0.3471
gnomAD - Genomes Other Sub 2146 C=0.5871 G=0.4129
The PAGE Study Global Study-wide 78698 C=0.58047 G=0.41953
The PAGE Study AfricanAmerican Sub 32514 C=0.46758 G=0.53242
The PAGE Study Mexican Sub 10810 C=0.77724 G=0.22276
The PAGE Study Asian Sub 8318 C=0.6518 G=0.3482
The PAGE Study PuertoRican Sub 7918 C=0.5724 G=0.4276
The PAGE Study NativeHawaiian Sub 4534 C=0.6367 G=0.3633
The PAGE Study Cuban Sub 4230 C=0.6095 G=0.3905
The PAGE Study Dominican Sub 3826 C=0.5384 G=0.4616
The PAGE Study CentralAmerican Sub 2450 C=0.7518 G=0.2482
The PAGE Study SouthAmerican Sub 1982 C=0.7699 G=0.2301
The PAGE Study NativeAmerican Sub 1260 C=0.6325 G=0.3675
The PAGE Study SouthAsian Sub 856 C=0.506 G=0.494
8.3KJPN JAPANESE Study-wide 16758 C=0.65378 G=0.34622
GO Exome Sequencing Project Global Study-wide 12998 C=0.55570 G=0.44430
GO Exome Sequencing Project European American Sub 8596 C=0.6025 G=0.3975
GO Exome Sequencing Project African American Sub 4402 C=0.4643 G=0.5357
1000Genomes Global Study-wide 5008 C=0.5745 G=0.4255
1000Genomes African Sub 1322 C=0.4160 G=0.5840
1000Genomes East Asian Sub 1008 C=0.6954 G=0.3046
1000Genomes Europe Sub 1006 C=0.6173 G=0.3827
1000Genomes South Asian Sub 978 C=0.508 G=0.492
1000Genomes American Sub 694 C=0.732 G=0.268
Genetic variation in the Estonian population Estonian Study-wide 4480 C=0.6315 G=0.3685
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 C=0.6066 G=0.3934
UK 10K study - Twins TWIN COHORT Study-wide 3708 C=0.6073 G=0.3927
KOREAN population from KRGDB KOREAN Study-wide 2930 C=0.6372 G=0.3628
HapMap Global Study-wide 1892 C=0.5698 G=0.4302
HapMap American Sub 770 C=0.642 G=0.358
HapMap African Sub 692 C=0.429 G=0.571
HapMap Asian Sub 254 C=0.681 G=0.319
HapMap Europe Sub 176 C=0.648 G=0.352
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 C=0.609 G=0.391
CNV burdens in cranial meningiomas Global Study-wide 780 C=0.629 G=0.371
CNV burdens in cranial meningiomas CRM Sub 780 C=0.629 G=0.371
Northern Sweden ACPOP Study-wide 600 C=0.643 G=0.357
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 C=0.687 G=0.313
A Vietnamese Genetic Variation Database Global Study-wide 525 C=0.863 G=0.137
SGDP_PRJ Global Study-wide 330 C=0.376 G=0.624
FINRISK Finnish from FINRISK project Study-wide 304 C=0.645 G=0.355
Qatari Global Study-wide 216 C=0.579 G=0.421
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 82 C=0.68 G=0.32
The Danish reference pan genome Danish Study-wide 40 C=0.55 G=0.45
Siberian Global Study-wide 38 C=0.39 G=0.61
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 G
GRCh38.p13 chr 11 NC_000011.10:g.4546105= NC_000011.10:g.4546105C>A NC_000011.10:g.4546105C>G
GRCh37.p13 chr 11 NC_000011.9:g.4567335= NC_000011.9:g.4567335C>A NC_000011.9:g.4567335C>G
OR52M1 transcript NM_001004137.1:c.915= NM_001004137.1:c.915C>A NM_001004137.1:c.915C>G
olfactory receptor 52M1 NP_001004137.1:p.Ser305= NP_001004137.1:p.Ser305Arg NP_001004137.1:p.Ser305Arg
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#.

129 SubSNP, 27 Frequency submissions
No Submitter Submission ID Date (Build)
1 SC_JCM ss3747574 Sep 28, 2001 (100)
2 BCM_SSAHASNP ss10675132 Jul 11, 2003 (116)
3 SC_SNP ss16101930 Feb 27, 2004 (120)
4 CSHL-HAPMAP ss19215043 Feb 27, 2004 (120)
5 SSAHASNP ss20829419 Apr 05, 2004 (121)
6 PERLEGEN ss24066476 Sep 20, 2004 (123)
7 ABI ss39944984 Mar 15, 2006 (126)
8 ILLUMINA ss65727097 Oct 15, 2006 (127)
9 AFFY ss65927455 Nov 30, 2006 (127)
10 AFFY ss66110517 Nov 30, 2006 (127)
11 PERLEGEN ss69307182 May 17, 2007 (127)
12 ILLUMINA ss74877182 Dec 07, 2007 (129)
13 AFFY ss76089968 Dec 07, 2007 (129)
14 KRIBB_YJKIM ss81838798 Dec 14, 2007 (130)
15 HGSV ss84971214 Dec 14, 2007 (130)
16 CORNELL ss86239446 Mar 23, 2008 (129)
17 BCMHGSC_JDW ss88440140 Mar 23, 2008 (129)
18 BGI ss102933717 Dec 01, 2009 (131)
19 1000GENOMES ss114121607 Jan 25, 2009 (130)
20 ILLUMINA-UK ss118463604 Feb 14, 2009 (130)
21 ENSEMBL ss132001954 Dec 01, 2009 (131)
22 ENSEMBL ss132249652 Dec 01, 2009 (131)
23 SEATTLESEQ ss159722140 Dec 01, 2009 (131)
24 ILLUMINA ss160567281 Dec 01, 2009 (131)
25 COMPLETE_GENOMICS ss168910594 Jul 04, 2010 (132)
26 COMPLETE_GENOMICS ss170330432 Jul 04, 2010 (132)
27 AFFY ss172468617 Jul 04, 2010 (132)
28 ILLUMINA ss173420750 Jul 04, 2010 (132)
29 BUSHMAN ss202323390 Jul 04, 2010 (132)
30 1000GENOMES ss225060770 Jul 14, 2010 (132)
31 1000GENOMES ss235422759 Jul 15, 2010 (132)
32 1000GENOMES ss242081865 Jul 15, 2010 (132)
33 GMI ss280862168 May 04, 2012 (137)
34 GMI ss286304622 Apr 25, 2013 (138)
35 PJP ss291035666 May 09, 2011 (134)
36 NHLBI-ESP ss342315342 May 09, 2011 (134)
37 ILLUMINA ss480627965 May 04, 2012 (137)
38 ILLUMINA ss480642997 May 04, 2012 (137)
39 ILLUMINA ss481483315 Sep 08, 2015 (146)
40 ILLUMINA ss485109149 May 04, 2012 (137)
41 1000GENOMES ss491010369 May 04, 2012 (137)
42 EXOME_CHIP ss491444977 May 04, 2012 (137)
43 CLINSEQ_SNP ss491637767 May 04, 2012 (137)
44 ILLUMINA ss537113227 Sep 08, 2015 (146)
45 TISHKOFF ss562349195 Apr 25, 2013 (138)
46 SSMP ss657697319 Apr 25, 2013 (138)
47 ILLUMINA ss778342332 Aug 21, 2014 (142)
48 ILLUMINA ss780893517 Aug 21, 2014 (142)
49 ILLUMINA ss783000850 Aug 21, 2014 (142)
50 ILLUMINA ss783580157 Aug 21, 2014 (142)
51 ILLUMINA ss783961347 Aug 21, 2014 (142)
52 ILLUMINA ss832257973 Apr 01, 2015 (144)
53 ILLUMINA ss833796942 Aug 21, 2014 (142)
54 JMKIDD_LAB ss974477473 Aug 21, 2014 (142)
55 EVA-GONL ss988151590 Aug 21, 2014 (142)
56 JMKIDD_LAB ss1067519227 Aug 21, 2014 (142)
57 JMKIDD_LAB ss1077458855 Aug 21, 2014 (142)
58 1000GENOMES ss1339916024 Aug 21, 2014 (142)
59 DDI ss1426516569 Apr 01, 2015 (144)
60 EVA_GENOME_DK ss1575487685 Apr 01, 2015 (144)
61 EVA_FINRISK ss1584072300 Apr 01, 2015 (144)
62 EVA_UK10K_ALSPAC ss1625882935 Apr 01, 2015 (144)
63 EVA_UK10K_TWINSUK ss1668876968 Apr 01, 2015 (144)
64 EVA_EXAC ss1690214426 Apr 01, 2015 (144)
65 EVA_EXAC ss1690214427 Apr 01, 2015 (144)
66 EVA_MGP ss1711279933 Apr 01, 2015 (144)
67 EVA_SVP ss1713228632 Apr 01, 2015 (144)
68 ILLUMINA ss1752018349 Sep 08, 2015 (146)
69 HAMMER_LAB ss1806668017 Sep 08, 2015 (146)
70 WEILL_CORNELL_DGM ss1931515912 Feb 12, 2016 (147)
71 ILLUMINA ss1959318754 Feb 12, 2016 (147)
72 GENOMED ss1967276841 Jul 19, 2016 (147)
73 JJLAB ss2026497447 Sep 14, 2016 (149)
74 USC_VALOUEV ss2154784687 Dec 20, 2016 (150)
75 HUMAN_LONGEVITY ss2179785217 Dec 20, 2016 (150)
76 TOPMED ss2342933544 Dec 20, 2016 (150)
77 SYSTEMSBIOZJU ss2627717752 Nov 08, 2017 (151)
78 ILLUMINA ss2632793342 Nov 08, 2017 (151)
79 GRF ss2699054239 Nov 08, 2017 (151)
80 GNOMAD ss2748540751 Nov 08, 2017 (151)
81 GNOMAD ss2895777712 Nov 08, 2017 (151)
82 AFFY ss2984931464 Nov 08, 2017 (151)
83 SWEGEN ss3007512885 Nov 08, 2017 (151)
84 EVA_SAMSUNG_MC ss3023066281 Nov 08, 2017 (151)
85 BIOINF_KMB_FNS_UNIBA ss3027040671 Nov 08, 2017 (151)
86 TOPMED ss3135825312 Nov 08, 2017 (151)
87 CSHL ss3349426241 Nov 08, 2017 (151)
88 ILLUMINA ss3626585930 Oct 12, 2018 (152)
89 ILLUMINA ss3626585931 Oct 12, 2018 (152)
90 ILLUMINA ss3630813014 Oct 12, 2018 (152)
91 ILLUMINA ss3632973036 Oct 12, 2018 (152)
92 ILLUMINA ss3633671655 Oct 12, 2018 (152)
93 ILLUMINA ss3634436337 Oct 12, 2018 (152)
94 ILLUMINA ss3634436338 Oct 12, 2018 (152)
95 ILLUMINA ss3635363600 Oct 12, 2018 (152)
96 ILLUMINA ss3636121200 Oct 12, 2018 (152)
97 ILLUMINA ss3637114386 Oct 12, 2018 (152)
98 ILLUMINA ss3637887323 Oct 12, 2018 (152)
99 ILLUMINA ss3640143678 Oct 12, 2018 (152)
100 ILLUMINA ss3640143679 Oct 12, 2018 (152)
101 ILLUMINA ss3642887345 Oct 12, 2018 (152)
102 ILLUMINA ss3644552669 Oct 12, 2018 (152)
103 OMUKHERJEE_ADBS ss3646421055 Oct 12, 2018 (152)
104 URBANLAB ss3649519030 Oct 12, 2018 (152)
105 ILLUMINA ss3653703034 Oct 12, 2018 (152)
106 EGCUT_WGS ss3674908973 Jul 13, 2019 (153)
107 EVA_DECODE ss3691115539 Jul 13, 2019 (153)
108 ACPOP ss3737872982 Jul 13, 2019 (153)
109 ILLUMINA ss3744737274 Jul 13, 2019 (153)
110 ILLUMINA ss3744737275 Jul 13, 2019 (153)
111 EVA ss3748879510 Jul 13, 2019 (153)
112 PAGE_CC ss3771600300 Jul 13, 2019 (153)
113 ILLUMINA ss3772237418 Jul 13, 2019 (153)
114 KHV_HUMAN_GENOMES ss3814227173 Jul 13, 2019 (153)
115 EVA ss3824584442 Apr 26, 2020 (154)
116 EVA ss3825527135 Apr 26, 2020 (154)
117 EVA ss3825790757 Apr 26, 2020 (154)
118 EVA ss3832447604 Apr 26, 2020 (154)
119 SGDP_PRJ ss3875539225 Apr 26, 2020 (154)
120 KRGDB ss3923763242 Apr 26, 2020 (154)
121 FSA-LAB ss3983994325 Apr 26, 2021 (155)
122 EVA ss3984644897 Apr 26, 2021 (155)
123 EVA ss3985514282 Apr 26, 2021 (155)
124 EVA ss3986511833 Apr 26, 2021 (155)
125 EVA ss4017519963 Apr 26, 2021 (155)
126 TOPMED ss4873508754 Apr 26, 2021 (155)
127 TOMMO_GENOMICS ss5200465259 Apr 26, 2021 (155)
128 EVA ss5236890401 Apr 26, 2021 (155)
129 EVA ss5237212439 Apr 26, 2021 (155)
130 1000Genomes NC_000011.9 - 4567335 Oct 12, 2018 (152)
131 The Avon Longitudinal Study of Parents and Children NC_000011.9 - 4567335 Oct 12, 2018 (152)
132 Genetic variation in the Estonian population NC_000011.9 - 4567335 Oct 12, 2018 (152)
133 ExAC

Submission ignored due to conflicting rows:
Row 459220 (NC_000011.9:4567334:C:C 73129/120312, NC_000011.9:4567334:C:G 47183/120312)
Row 459221 (NC_000011.9:4567334:C:C 120311/120312, NC_000011.9:4567334:C:A 1/120312)

- Oct 12, 2018 (152)
134 ExAC

Submission ignored due to conflicting rows:
Row 459220 (NC_000011.9:4567334:C:C 73129/120312, NC_000011.9:4567334:C:G 47183/120312)
Row 459221 (NC_000011.9:4567334:C:C 120311/120312, NC_000011.9:4567334:C:A 1/120312)

- Oct 12, 2018 (152)
135 FINRISK NC_000011.9 - 4567335 Apr 26, 2020 (154)
136 The Danish reference pan genome NC_000011.9 - 4567335 Apr 26, 2020 (154)
137 gnomAD - Genomes NC_000011.10 - 4546105 Apr 26, 2021 (155)
138 gnomAD - Exomes

Submission ignored due to conflicting rows:
Row 7935917 (NC_000011.9:4567334:C:C 246513/246514, NC_000011.9:4567334:C:A 1/246514)
Row 7935919 (NC_000011.9:4567334:C:C 152621/246514, NC_000011.9:4567334:C:G 93893/246514)

- Jul 13, 2019 (153)
139 gnomAD - Exomes

Submission ignored due to conflicting rows:
Row 7935917 (NC_000011.9:4567334:C:C 246513/246514, NC_000011.9:4567334:C:A 1/246514)
Row 7935919 (NC_000011.9:4567334:C:C 152621/246514, NC_000011.9:4567334:C:G 93893/246514)

- Jul 13, 2019 (153)
140 GO Exome Sequencing Project NC_000011.9 - 4567335 Oct 12, 2018 (152)
141 Genome of the Netherlands Release 5 NC_000011.9 - 4567335 Apr 26, 2020 (154)
142 HapMap NC_000011.10 - 4546105 Apr 26, 2020 (154)
143 KOREAN population from KRGDB NC_000011.9 - 4567335 Apr 26, 2020 (154)
144 Medical Genome Project healthy controls from Spanish population NC_000011.9 - 4567335 Apr 26, 2020 (154)
145 Northern Sweden NC_000011.9 - 4567335 Jul 13, 2019 (153)
146 The PAGE Study NC_000011.10 - 4546105 Jul 13, 2019 (153)
147 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000011.9 - 4567335 Apr 26, 2021 (155)
148 CNV burdens in cranial meningiomas NC_000011.9 - 4567335 Apr 26, 2021 (155)
149 Qatari NC_000011.9 - 4567335 Apr 26, 2020 (154)
150 SGDP_PRJ NC_000011.9 - 4567335 Apr 26, 2020 (154)
151 Siberian NC_000011.9 - 4567335 Apr 26, 2020 (154)
152 8.3KJPN NC_000011.9 - 4567335 Apr 26, 2021 (155)
153 TopMed NC_000011.10 - 4546105 Apr 26, 2021 (155)
154 UK 10K study - Twins NC_000011.9 - 4567335 Oct 12, 2018 (152)
155 A Vietnamese Genetic Variation Database NC_000011.9 - 4567335 Jul 13, 2019 (153)
156 ALFA NC_000011.10 - 4546105 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)
rs56688099 Feb 26, 2009 (130)
rs57297503 May 23, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss1690214427 NC_000011.9:4567334:C:A NC_000011.10:4546104:C:A (self)
ss66110517, ss76089968, ss84971214, ss88440140, ss114121607, ss118463604, ss168910594, ss170330432, ss172468617, ss202323390, ss280862168, ss286304622, ss291035666, ss480627965, ss491637767, ss1713228632, ss3642887345 NC_000011.8:4523910:C:G NC_000011.10:4546104:C:G (self)
52391595, 29099009, 20647221, 68761, 2418375, 1042097, 12971965, 30940636, 395693, 11157847, 740209, 194371, 13557842, 27556205, 7301041, 58434566, 29099009, 6458032, ss225060770, ss235422759, ss242081865, ss342315342, ss480642997, ss481483315, ss485109149, ss491010369, ss491444977, ss537113227, ss562349195, ss657697319, ss778342332, ss780893517, ss783000850, ss783580157, ss783961347, ss832257973, ss833796942, ss974477473, ss988151590, ss1067519227, ss1077458855, ss1339916024, ss1426516569, ss1575487685, ss1584072300, ss1625882935, ss1668876968, ss1690214426, ss1711279933, ss1752018349, ss1806668017, ss1931515912, ss1959318754, ss1967276841, ss2026497447, ss2154784687, ss2342933544, ss2627717752, ss2632793342, ss2699054239, ss2748540751, ss2895777712, ss2984931464, ss3007512885, ss3023066281, ss3349426241, ss3626585930, ss3626585931, ss3630813014, ss3632973036, ss3633671655, ss3634436337, ss3634436338, ss3635363600, ss3636121200, ss3637114386, ss3637887323, ss3640143678, ss3640143679, ss3644552669, ss3646421055, ss3653703034, ss3674908973, ss3737872982, ss3744737274, ss3744737275, ss3748879510, ss3772237418, ss3824584442, ss3825527135, ss3825790757, ss3832447604, ss3875539225, ss3923763242, ss3983994325, ss3984644897, ss3985514282, ss3986511833, ss4017519963, ss5200465259 NC_000011.9:4567334:C:G NC_000011.10:4546104:C:G (self)
369958635, 536454, 821769, 55921773, 89054410, 9635468488, ss2179785217, ss3027040671, ss3135825312, ss3649519030, ss3691115539, ss3771600300, ss3814227173, ss4873508754, ss5236890401, ss5237212439 NC_000011.10:4546104:C:G NC_000011.10:4546104:C:G (self)
ss16101930, ss19215043, ss20829419 NT_009237.16:3331274:C:G NC_000011.10:4546104:C:G (self)
ss3747574, ss24066476, ss39944984, ss65727097, ss65927455, ss69307182, ss74877182, ss81838798, ss86239446, ss102933717, ss132001954, ss132249652, ss159722140, ss160567281, ss173420750 NT_009237.18:4507334:C:G NC_000011.10:4546104:C:G (self)
ss10675132 NT_028310.10:3327507:C:G NC_000011.10:4546104:C: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 rs2657167

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