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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.

rs2735842

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr7:129206628 (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
A>G
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.221701 (58682/264690, TOPMED)
A=0.203075 (50188/247140, GnomAD_exome)
A=0.214385 (30022/140038, GnomAD) (+ 21 more)
A=0.202883 (24395/120242, ExAC)
A=0.17632 (16286/92366, ALFA)
A=0.26507 (4442/16758, 8.3KJPN)
A=0.21052 (2738/13006, GO-ESP)
A=0.2468 (1236/5008, 1000G)
A=0.1458 (653/4480, Estonian)
A=0.1632 (629/3854, ALSPAC)
A=0.1677 (622/3708, TWINSUK)
A=0.2755 (806/2926, KOREAN)
A=0.2375 (495/2084, HGDP_Stanford)
A=0.2254 (426/1890, HapMap)
A=0.168 (168/998, GoNL)
A=0.175 (105/600, NorthernSweden)
A=0.339 (181/534, MGP)
A=0.214 (106/496, SGDP_PRJ)
A=0.348 (161/463, Vietnamese)
A=0.220 (67/304, FINRISK)
A=0.130 (28/216, Qatari)
A=0.17 (14/82, Ancient Sardinia)
A=0.23 (12/52, Siberian)
A=0.07 (3/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
SMO : 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 7 NC_000007.14:g.129206628A>G
GRCh37.p13 chr 7 NC_000007.13:g.128846469A>G
SMO RefSeqGene (LRG_1393) NG_023340.2:g.22757A>G
Gene: SMO, smoothened, frizzled class receptor (plus strand)
Molecule type Change Amino acid[Codon] SO Term
SMO transcript NM_005631.5:c.1264+41A>G N/A Intron Variant
SMO transcript variant X1 XM_024446891.1:c.874+41A>G 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

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 92366 A=0.17632 G=0.82368
European Sub 70216 A=0.15417 G=0.84583
African Sub 8440 A=0.3060 G=0.6940
African Others Sub 274 A=0.350 G=0.650
African American Sub 8166 A=0.3046 G=0.6954
Asian Sub 294 A=0.265 G=0.735
East Asian Sub 190 A=0.253 G=0.747
Other Asian Sub 104 A=0.288 G=0.712
Latin American 1 Sub 400 A=0.180 G=0.820
Latin American 2 Sub 3376 A=0.2470 G=0.7530
South Asian Sub 4968 A=0.2140 G=0.7860
Other Sub 4672 A=0.1779 G=0.8221


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 A=0.221701 G=0.778299
gnomAD - Exomes Global Study-wide 247140 A=0.203075 G=0.796925
gnomAD - Exomes European Sub 132816 A=0.163459 G=0.836541
gnomAD - Exomes Asian Sub 48184 A=0.23792 G=0.76208
gnomAD - Exomes American Sub 34156 A=0.28291 G=0.71709
gnomAD - Exomes African Sub 16230 A=0.31220 G=0.68780
gnomAD - Exomes Ashkenazi Jewish Sub 9730 A=0.1307 G=0.8693
gnomAD - Exomes Other Sub 6024 A=0.1680 G=0.8320
gnomAD - Genomes Global Study-wide 140038 A=0.214385 G=0.785615
gnomAD - Genomes European Sub 75894 A=0.15781 G=0.84219
gnomAD - Genomes African Sub 41914 A=0.30775 G=0.69225
gnomAD - Genomes American Sub 13632 A=0.25954 G=0.74046
gnomAD - Genomes Ashkenazi Jewish Sub 3324 A=0.1224 G=0.8776
gnomAD - Genomes East Asian Sub 3124 A=0.2484 G=0.7516
gnomAD - Genomes Other Sub 2150 A=0.1977 G=0.8023
ExAC Global Study-wide 120242 A=0.202883 G=0.797117
ExAC Europe Sub 73006 A=0.16452 G=0.83548
ExAC Asian Sub 24388 A=0.23479 G=0.76521
ExAC American Sub 11556 A=0.28609 G=0.71391
ExAC African Sub 10388 A=0.30641 G=0.69359
ExAC Other Sub 904 A=0.187 G=0.813
8.3KJPN JAPANESE Study-wide 16758 A=0.26507 G=0.73493
GO Exome Sequencing Project Global Study-wide 13006 A=0.21052 G=0.78948
GO Exome Sequencing Project European American Sub 8600 A=0.1609 G=0.8391
GO Exome Sequencing Project African American Sub 4406 A=0.3073 G=0.6927
1000Genomes Global Study-wide 5008 A=0.2468 G=0.7532
1000Genomes African Sub 1322 A=0.3306 G=0.6694
1000Genomes East Asian Sub 1008 A=0.2440 G=0.7560
1000Genomes Europe Sub 1006 A=0.1769 G=0.8231
1000Genomes South Asian Sub 978 A=0.234 G=0.766
1000Genomes American Sub 694 A=0.210 G=0.790
Genetic variation in the Estonian population Estonian Study-wide 4480 A=0.1458 G=0.8542
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 A=0.1632 G=0.8368
UK 10K study - Twins TWIN COHORT Study-wide 3708 A=0.1677 G=0.8323
KOREAN population from KRGDB KOREAN Study-wide 2926 A=0.2755 G=0.7245
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 A=0.2375 G=0.7625
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 A=0.332 G=0.668
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 A=0.196 G=0.804
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 A=0.120 G=0.880
HGDP-CEPH-db Supplement 1 Europe Sub 320 A=0.134 G=0.866
HGDP-CEPH-db Supplement 1 Africa Sub 242 A=0.326 G=0.674
HGDP-CEPH-db Supplement 1 America Sub 216 A=0.269 G=0.731
HGDP-CEPH-db Supplement 1 Oceania Sub 72 A=0.50 G=0.50
HapMap Global Study-wide 1890 A=0.2254 G=0.7746
HapMap American Sub 770 A=0.209 G=0.791
HapMap African Sub 690 A=0.270 G=0.730
HapMap Asian Sub 254 A=0.220 G=0.780
HapMap Europe Sub 176 A=0.131 G=0.869
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 A=0.168 G=0.832
Northern Sweden ACPOP Study-wide 600 A=0.175 G=0.825
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 A=0.339 G=0.661
SGDP_PRJ Global Study-wide 496 A=0.214 G=0.786
A Vietnamese Genetic Variation Database Global Study-wide 463 A=0.348 G=0.652
FINRISK Finnish from FINRISK project Study-wide 304 A=0.220 G=0.780
Qatari Global Study-wide 216 A=0.130 G=0.870
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 82 A=0.17 G=0.83
Siberian Global Study-wide 52 A=0.23 G=0.77
The Danish reference pan genome Danish Study-wide 40 A=0.07 G=0.93
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 A= G
GRCh38.p13 chr 7 NC_000007.14:g.129206628= NC_000007.14:g.129206628A>G
GRCh37.p13 chr 7 NC_000007.13:g.128846469= NC_000007.13:g.128846469A>G
SMO RefSeqGene (LRG_1393) NG_023340.2:g.22757= NG_023340.2:g.22757A>G
SMO transcript NM_005631.4:c.1264+41= NM_005631.4:c.1264+41A>G
SMO transcript NM_005631.5:c.1264+41= NM_005631.5:c.1264+41A>G
SMO transcript variant X1 XM_024446891.1:c.874+41= XM_024446891.1:c.874+41A>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#.

118 SubSNP, 24 Frequency submissions
No Submitter Submission ID Date (Build)
1 SC_JCM ss3862101 Sep 28, 2001 (100)
2 WI_SSAHASNP ss6521825 Feb 20, 2003 (111)
3 CSHL-HAPMAP ss17155698 Feb 27, 2004 (120)
4 CSHL-HAPMAP ss19700901 Feb 27, 2004 (120)
5 SSAHASNP ss22551899 Apr 05, 2004 (121)
6 PERLEGEN ss23764479 Sep 20, 2004 (123)
7 ABI ss44807409 Mar 13, 2006 (126)
8 SI_EXO ss52076305 Oct 14, 2006 (127)
9 ILLUMINA ss66679266 Nov 30, 2006 (127)
10 ILLUMINA ss67270801 Nov 30, 2006 (127)
11 ILLUMINA ss67671395 Nov 30, 2006 (127)
12 PERLEGEN ss69027939 May 17, 2007 (127)
13 ILLUMINA ss70749256 May 27, 2008 (130)
14 ILLUMINA ss71321410 May 17, 2007 (127)
15 ILLUMINA ss75884477 Dec 06, 2007 (129)
16 AFFY ss76730891 Dec 08, 2007 (130)
17 CGM_KYOTO ss76863600 Dec 06, 2007 (129)
18 ILLUMINA ss79145387 Dec 16, 2007 (130)
19 KRIBB_YJKIM ss84074937 Dec 16, 2007 (130)
20 HGSV ss85070975 Dec 16, 2007 (130)
21 HGSV ss86113969 Dec 16, 2007 (130)
22 BCMHGSC_JDW ss93765177 Mar 25, 2008 (129)
23 HUMANGENOME_JCVI ss98336000 Feb 06, 2009 (130)
24 BGI ss105572641 Feb 06, 2009 (130)
25 1000GENOMES ss112527990 Jan 25, 2009 (130)
26 1000GENOMES ss114424967 Jan 25, 2009 (130)
27 ILLUMINA ss122096066 Dec 01, 2009 (131)
28 ENSEMBL ss142926514 Dec 01, 2009 (131)
29 ILLUMINA ss154231449 Dec 01, 2009 (131)
30 GMI ss155491618 Dec 01, 2009 (131)
31 ILLUMINA ss159407949 Dec 01, 2009 (131)
32 COMPLETE_GENOMICS ss162713520 Jul 04, 2010 (132)
33 COMPLETE_GENOMICS ss165390897 Jul 04, 2010 (132)
34 COMPLETE_GENOMICS ss167105188 Jul 04, 2010 (132)
35 ILLUMINA ss171362268 Jul 04, 2010 (132)
36 ILLUMINA ss173448110 Jul 04, 2010 (132)
37 BUSHMAN ss198265228 Jul 04, 2010 (132)
38 BCM-HGSC-SUB ss208338050 Jul 04, 2010 (132)
39 1000GENOMES ss223329991 Jul 14, 2010 (132)
40 1000GENOMES ss234166261 Jul 15, 2010 (132)
41 1000GENOMES ss241080076 Jul 15, 2010 (132)
42 BL ss254673600 May 09, 2011 (134)
43 GMI ss279529944 May 04, 2012 (137)
44 GMI ss285718077 Apr 25, 2013 (138)
45 PJP ss293965331 May 09, 2011 (134)
46 1000GENOMES ss490954116 May 04, 2012 (137)
47 CLINSEQ_SNP ss491914936 May 04, 2012 (137)
48 ILLUMINA ss535962340 Sep 08, 2015 (146)
49 TISHKOFF ss560302524 Apr 25, 2013 (138)
50 SSMP ss654712227 Apr 25, 2013 (138)
51 NHLBI-ESP ss712807308 Apr 25, 2013 (138)
52 ILLUMINA ss825475905 Apr 01, 2015 (144)
53 ILLUMINA ss832919639 Aug 21, 2014 (142)
54 ILLUMINA ss833510469 Aug 21, 2014 (142)
55 JMKIDD_LAB ss974465812 Aug 21, 2014 (142)
56 EVA-GONL ss984797325 Aug 21, 2014 (142)
57 JMKIDD_LAB ss1067492068 Aug 21, 2014 (142)
58 JMKIDD_LAB ss1074980850 Aug 21, 2014 (142)
59 1000GENOMES ss1327137068 Aug 21, 2014 (142)
60 DDI ss1431279091 Apr 01, 2015 (144)
61 EVA_GENOME_DK ss1582401246 Apr 01, 2015 (144)
62 EVA_FINRISK ss1584055014 Apr 01, 2015 (144)
63 EVA_DECODE ss1594385949 Apr 01, 2015 (144)
64 EVA_UK10K_ALSPAC ss1619214439 Apr 01, 2015 (144)
65 EVA_UK10K_TWINSUK ss1662208472 Apr 01, 2015 (144)
66 EVA_EXAC ss1688944506 Apr 01, 2015 (144)
67 EVA_MGP ss1711179675 Apr 01, 2015 (144)
68 EVA_SVP ss1712987237 Apr 01, 2015 (144)
69 HAMMER_LAB ss1805218552 Sep 08, 2015 (146)
70 WEILL_CORNELL_DGM ss1928055205 Feb 12, 2016 (147)
71 GENOMED ss1966658518 Feb 12, 2016 (147)
72 JJLAB ss2024715940 Sep 14, 2016 (149)
73 USC_VALOUEV ss2152936846 Dec 20, 2016 (150)
74 HUMAN_LONGEVITY ss2297854775 Dec 20, 2016 (150)
75 TOPMED ss2467340764 Dec 20, 2016 (150)
76 SYSTEMSBIOZJU ss2626845615 Nov 08, 2017 (151)
77 GRF ss2708655299 Nov 08, 2017 (151)
78 GNOMAD ss2736763775 Nov 08, 2017 (151)
79 GNOMAD ss2747922953 Nov 08, 2017 (151)
80 GNOMAD ss2859112524 Nov 08, 2017 (151)
81 AFFY ss2985420545 Nov 08, 2017 (151)
82 AFFY ss2986052674 Nov 08, 2017 (151)
83 SWEGEN ss3002033363 Nov 08, 2017 (151)
84 BIOINF_KMB_FNS_UNIBA ss3026146901 Nov 08, 2017 (151)
85 CSHL ss3347843251 Nov 08, 2017 (151)
86 TOPMED ss3544415975 Nov 08, 2017 (151)
87 ILLUMINA ss3629913255 Oct 12, 2018 (152)
88 ILLUMINA ss3638723627 Oct 12, 2018 (152)
89 ILLUMINA ss3639363066 Oct 12, 2018 (152)
90 ILLUMINA ss3639710413 Oct 12, 2018 (152)
91 ILLUMINA ss3643657453 Oct 12, 2018 (152)
92 OMUKHERJEE_ADBS ss3646363517 Oct 12, 2018 (152)
93 URBANLAB ss3648752050 Oct 12, 2018 (152)
94 ILLUMINA ss3654181615 Oct 12, 2018 (152)
95 EGCUT_WGS ss3669789560 Jul 13, 2019 (153)
96 EVA_DECODE ss3720690866 Jul 13, 2019 (153)
97 ACPOP ss3735071150 Jul 13, 2019 (153)
98 EVA ss3767160193 Jul 13, 2019 (153)
99 PACBIO ss3785957468 Jul 13, 2019 (153)
100 PACBIO ss3791236463 Jul 13, 2019 (153)
101 PACBIO ss3796116613 Jul 13, 2019 (153)
102 KHV_HUMAN_GENOMES ss3810330165 Jul 13, 2019 (153)
103 EVA ss3824317279 Apr 26, 2020 (154)
104 EVA ss3825728678 Apr 26, 2020 (154)
105 EVA ss3830819634 Apr 26, 2020 (154)
106 EVA ss3838908812 Apr 26, 2020 (154)
107 EVA ss3844365241 Apr 26, 2020 (154)
108 HGDP ss3847890809 Apr 26, 2020 (154)
109 SGDP_PRJ ss3868398288 Apr 26, 2020 (154)
110 KRGDB ss3915745140 Apr 26, 2020 (154)
111 FSA-LAB ss3984380171 Apr 26, 2021 (155)
112 FSA-LAB ss3984380172 Apr 26, 2021 (155)
113 EVA ss3985321469 Apr 26, 2021 (155)
114 EVA ss3986399204 Apr 26, 2021 (155)
115 EVA ss4017359059 Apr 26, 2021 (155)
116 TOPMED ss4763774631 Apr 26, 2021 (155)
117 TOMMO_GENOMICS ss5185583117 Apr 26, 2021 (155)
118 EVA ss5237198211 Apr 26, 2021 (155)
119 1000Genomes NC_000007.13 - 128846469 Oct 12, 2018 (152)
120 The Avon Longitudinal Study of Parents and Children NC_000007.13 - 128846469 Oct 12, 2018 (152)
121 Genetic variation in the Estonian population NC_000007.13 - 128846469 Oct 12, 2018 (152)
122 ExAC NC_000007.13 - 128846469 Oct 12, 2018 (152)
123 FINRISK NC_000007.13 - 128846469 Apr 26, 2020 (154)
124 The Danish reference pan genome NC_000007.13 - 128846469 Apr 26, 2020 (154)
125 gnomAD - Genomes NC_000007.14 - 129206628 Apr 26, 2021 (155)
126 gnomAD - Exomes NC_000007.13 - 128846469 Jul 13, 2019 (153)
127 GO Exome Sequencing Project NC_000007.13 - 128846469 Oct 12, 2018 (152)
128 Genome of the Netherlands Release 5 NC_000007.13 - 128846469 Apr 26, 2020 (154)
129 HGDP-CEPH-db Supplement 1 NC_000007.12 - 128633705 Apr 26, 2020 (154)
130 HapMap NC_000007.14 - 129206628 Apr 26, 2020 (154)
131 KOREAN population from KRGDB NC_000007.13 - 128846469 Apr 26, 2020 (154)
132 Medical Genome Project healthy controls from Spanish population NC_000007.13 - 128846469 Apr 26, 2020 (154)
133 Northern Sweden NC_000007.13 - 128846469 Jul 13, 2019 (153)
134 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000007.13 - 128846469 Apr 26, 2021 (155)
135 Qatari NC_000007.13 - 128846469 Apr 26, 2020 (154)
136 SGDP_PRJ NC_000007.13 - 128846469 Apr 26, 2020 (154)
137 Siberian NC_000007.13 - 128846469 Apr 26, 2020 (154)
138 8.3KJPN NC_000007.13 - 128846469 Apr 26, 2021 (155)
139 TopMed NC_000007.14 - 129206628 Apr 26, 2021 (155)
140 UK 10K study - Twins NC_000007.13 - 128846469 Oct 12, 2018 (152)
141 A Vietnamese Genetic Variation Database NC_000007.13 - 128846469 Jul 13, 2019 (153)
142 ALFA NC_000007.14 - 129206628 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)
rs56605140 May 27, 2008 (130)
rs61682977 May 27, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss85070975, ss86113969, ss3639363066, ss3639710413 NC_000007.11:128440419:A:G NC_000007.14:129206627:A:G (self)
568701, ss93765177, ss112527990, ss114424967, ss162713520, ss165390897, ss167105188, ss198265228, ss208338050, ss254673600, ss279529944, ss285718077, ss293965331, ss491914936, ss825475905, ss1594385949, ss1712987237, ss3643657453, ss3847890809 NC_000007.12:128633704:A:G NC_000007.14:129206627:A:G (self)
39180803, 21798893, 15527808, 9026491, 51475, 8566184, 5927655, 775162, 9727985, 22922534, 295435, 8356015, 547396, 10097135, 20415268, 5453200, 43552424, 21798893, 4856724, ss223329991, ss234166261, ss241080076, ss490954116, ss535962340, ss560302524, ss654712227, ss712807308, ss832919639, ss833510469, ss974465812, ss984797325, ss1067492068, ss1074980850, ss1327137068, ss1431279091, ss1582401246, ss1584055014, ss1619214439, ss1662208472, ss1688944506, ss1711179675, ss1805218552, ss1928055205, ss1966658518, ss2024715940, ss2152936846, ss2467340764, ss2626845615, ss2708655299, ss2736763775, ss2747922953, ss2859112524, ss2985420545, ss2986052674, ss3002033363, ss3347843251, ss3629913255, ss3638723627, ss3646363517, ss3654181615, ss3669789560, ss3735071150, ss3767160193, ss3785957468, ss3791236463, ss3796116613, ss3824317279, ss3825728678, ss3830819634, ss3838908812, ss3868398288, ss3915745140, ss3984380171, ss3984380172, ss3985321469, ss3986399204, ss4017359059, ss5185583117 NC_000007.13:128846468:A:G NC_000007.14:129206627:A:G (self)
276659936, 3493473, 375915821, 601152190, 8315947139, ss2297854775, ss3026146901, ss3544415975, ss3648752050, ss3720690866, ss3810330165, ss3844365241, ss4763774631, ss5237198211 NC_000007.14:129206627:A:G NC_000007.14:129206627:A:G (self)
ss17155698, ss19700901, ss22551899 NT_007933.13:54022624:A:G NC_000007.14:129206627:A:G (self)
ss52076305 NT_007933.14:54030044:A:G NC_000007.14:129206627:A:G (self)
ss3862101, ss6521825, ss23764479, ss44807409, ss66679266, ss67270801, ss67671395, ss69027939, ss70749256, ss71321410, ss75884477, ss76730891, ss76863600, ss79145387, ss84074937, ss98336000, ss105572641, ss122096066, ss142926514, ss154231449, ss155491618, ss159407949, ss171362268, ss173448110 NT_007933.15:66879311:A:G NC_000007.14:129206627:A: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 rs2735842

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