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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.

rs7473

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr1:183145499 (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 / G>T
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.473233 (125260/264690, TOPMED)
G=0.446507 (72635/162674, ALFA)
G=0.475520 (66433/139706, GnomAD) (+ 19 more)
G=0.38091 (10763/28256, 14KJPN)
G=0.38365 (6430/16760, 8.3KJPN)
G=0.4558 (2919/6404, 1000G_30x)
G=0.4527 (2267/5008, 1000G)
G=0.4656 (2086/4480, Estonian)
G=0.4333 (1670/3854, ALSPAC)
G=0.4328 (1605/3708, TWINSUK)
G=0.4007 (1174/2930, KOREAN)
G=0.4713 (888/1884, HapMap)
G=0.4132 (757/1832, Korea1K)
G=0.443 (442/998, GoNL)
G=0.480 (288/600, NorthernSweden)
G=0.444 (237/534, MGP)
G=0.259 (118/456, SGDP_PRJ)
G=0.486 (105/216, Qatari)
G=0.374 (80/214, Vietnamese)
G=0.41 (28/68, Ancient Sardinia)
G=0.45 (18/40, GENOME_DK)
G=0.17 (6/36, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
LAMC1 : 3 Prime UTR Variant
Publications
2 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 162674 G=0.446507 A=0.553493, T=0.000000
European Sub 142030 G=0.446652 A=0.553348, T=0.000000
African Sub 6336 G=0.5934 A=0.4066, T=0.0000
African Others Sub 224 G=0.594 A=0.406, T=0.000
African American Sub 6112 G=0.5934 A=0.4066, T=0.0000
Asian Sub 674 G=0.355 A=0.645, T=0.000
East Asian Sub 542 G=0.376 A=0.624, T=0.000
Other Asian Sub 132 G=0.265 A=0.735, T=0.000
Latin American 1 Sub 750 G=0.471 A=0.529, T=0.000
Latin American 2 Sub 6274 G=0.3052 A=0.6948, T=0.0000
South Asian Sub 184 G=0.391 A=0.609, T=0.000
Other Sub 6426 G=0.4448 A=0.5552, 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 G=0.473233 A=0.526767
Allele Frequency Aggregator Total Global 162674 G=0.446507 A=0.553493, T=0.000000
Allele Frequency Aggregator European Sub 142030 G=0.446652 A=0.553348, T=0.000000
Allele Frequency Aggregator Other Sub 6426 G=0.4448 A=0.5552, T=0.0000
Allele Frequency Aggregator African Sub 6336 G=0.5934 A=0.4066, T=0.0000
Allele Frequency Aggregator Latin American 2 Sub 6274 G=0.3052 A=0.6948, T=0.0000
Allele Frequency Aggregator Latin American 1 Sub 750 G=0.471 A=0.529, T=0.000
Allele Frequency Aggregator Asian Sub 674 G=0.355 A=0.645, T=0.000
Allele Frequency Aggregator South Asian Sub 184 G=0.391 A=0.609, T=0.000
gnomAD - Genomes Global Study-wide 139706 G=0.475520 A=0.524480
gnomAD - Genomes European Sub 75714 G=0.43977 A=0.56023
gnomAD - Genomes African Sub 41800 G=0.57895 A=0.42105
gnomAD - Genomes American Sub 13602 G=0.38061 A=0.61939
gnomAD - Genomes Ashkenazi Jewish Sub 3320 G=0.4819 A=0.5181
gnomAD - Genomes East Asian Sub 3128 G=0.3910 A=0.6090
gnomAD - Genomes Other Sub 2142 G=0.4370 A=0.5630
14KJPN JAPANESE Study-wide 28256 G=0.38091 A=0.61909
8.3KJPN JAPANESE Study-wide 16760 G=0.38365 A=0.61635
1000Genomes_30x Global Study-wide 6404 G=0.4558 A=0.5442
1000Genomes_30x African Sub 1786 G=0.6041 A=0.3959
1000Genomes_30x Europe Sub 1266 G=0.4408 A=0.5592
1000Genomes_30x South Asian Sub 1202 G=0.4068 A=0.5932
1000Genomes_30x East Asian Sub 1170 G=0.3803 A=0.6197
1000Genomes_30x American Sub 980 G=0.355 A=0.645
1000Genomes Global Study-wide 5008 G=0.4527 A=0.5473
1000Genomes African Sub 1322 G=0.6014 A=0.3986
1000Genomes East Asian Sub 1008 G=0.3780 A=0.6220
1000Genomes Europe Sub 1006 G=0.4334 A=0.5666
1000Genomes South Asian Sub 978 G=0.411 A=0.589
1000Genomes American Sub 694 G=0.365 A=0.635
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.4656 A=0.5344
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.4333 A=0.5667
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.4328 A=0.5672
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.4007 A=0.5993
HapMap Global Study-wide 1884 G=0.4713 A=0.5287
HapMap American Sub 766 G=0.419 A=0.581
HapMap African Sub 692 G=0.542 A=0.458
HapMap Asian Sub 252 G=0.440 A=0.560
HapMap Europe Sub 174 G=0.466 A=0.534
Korean Genome Project KOREAN Study-wide 1832 G=0.4132 A=0.5868
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.443 A=0.557
Northern Sweden ACPOP Study-wide 600 G=0.480 A=0.520
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 G=0.444 A=0.556
SGDP_PRJ Global Study-wide 456 G=0.259 A=0.741
Qatari Global Study-wide 216 G=0.486 A=0.514
A Vietnamese Genetic Variation Database Global Study-wide 214 G=0.374 A=0.626
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 68 G=0.41 A=0.59
The Danish reference pan genome Danish Study-wide 40 G=0.45 A=0.55
Siberian Global Study-wide 36 G=0.17 A=0.83
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 1 NC_000001.11:g.183145499G>A
GRCh38.p14 chr 1 NC_000001.11:g.183145499G>T
GRCh37.p13 chr 1 NC_000001.10:g.183114634G>A
GRCh37.p13 chr 1 NC_000001.10:g.183114634G>T
LAMC1 RefSeqGene NG_011463.1:g.127040G>A
LAMC1 RefSeqGene NG_011463.1:g.127040G>T
Gene: LAMC1, laminin subunit gamma 1 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
LAMC1 transcript NM_002293.4:c.*2709= N/A 3 Prime UTR 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 T
GRCh38.p14 chr 1 NC_000001.11:g.183145499= NC_000001.11:g.183145499G>A NC_000001.11:g.183145499G>T
GRCh37.p13 chr 1 NC_000001.10:g.183114634= NC_000001.10:g.183114634G>A NC_000001.10:g.183114634G>T
LAMC1 RefSeqGene NG_011463.1:g.127040= NG_011463.1:g.127040G>A NG_011463.1:g.127040G>T
LAMC1 transcript NM_002293.4:c.*2709= NM_002293.4:c.*2709G>A NM_002293.4:c.*2709G>T
LAMC1 transcript NM_002293.3:c.*2709= NM_002293.3:c.*2709G>A NM_002293.3:c.*2709G>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#.

115 SubSNP, 22 Frequency submissions
No Submitter Submission ID Date (Build)
1 LEE ss1554741 Oct 05, 2000 (110)
2 TSC-CSHL ss2379006 Oct 23, 2000 (110)
3 LEE ss4436131 May 29, 2002 (110)
4 YUSUKE ss4924826 Aug 28, 2002 (110)
5 CSHL-HAPMAP ss16400450 Feb 27, 2004 (120)
6 SSAHASNP ss20582382 Apr 05, 2004 (121)
7 PERLEGEN ss23853351 Sep 20, 2004 (123)
8 ABI ss43869276 Mar 14, 2006 (126)
9 ILLUMINA ss65739652 Oct 13, 2006 (127)
10 ILLUMINA ss74856631 Dec 07, 2007 (129)
11 BCMHGSC_JDW ss87892934 Mar 23, 2008 (129)
12 KRIBB_YJKIM ss102643995 Feb 05, 2009 (130)
13 1000GENOMES ss108757795 Jan 23, 2009 (130)
14 1000GENOMES ss111450413 Jan 25, 2009 (130)
15 ENSEMBL ss138116111 Dec 01, 2009 (131)
16 ENSEMBL ss144237558 Dec 01, 2009 (131)
17 GMI ss156005571 Dec 01, 2009 (131)
18 ILLUMINA ss160880942 Dec 01, 2009 (131)
19 COMPLETE_GENOMICS ss164602958 Jul 04, 2010 (132)
20 COMPLETE_GENOMICS ss165527817 Jul 04, 2010 (132)
21 COMPLETE_GENOMICS ss167349025 Jul 04, 2010 (132)
22 ILLUMINA ss174379922 Jul 04, 2010 (132)
23 BUSHMAN ss199333775 Jul 04, 2010 (132)
24 BCM-HGSC-SUB ss205234450 Jul 04, 2010 (132)
25 1000GENOMES ss218757215 Jul 14, 2010 (132)
26 1000GENOMES ss230810192 Jul 14, 2010 (132)
27 1000GENOMES ss238440401 Jul 15, 2010 (132)
28 BL ss253657738 May 09, 2011 (134)
29 GMI ss276127318 May 04, 2012 (137)
30 PJP ss290677666 May 09, 2011 (134)
31 ILLUMINA ss481570398 May 04, 2012 (137)
32 ILLUMINA ss481600171 May 04, 2012 (137)
33 ILLUMINA ss482571819 Sep 08, 2015 (146)
34 ILLUMINA ss485580242 May 04, 2012 (137)
35 ILLUMINA ss537473483 Sep 08, 2015 (146)
36 SSMP ss648544752 Apr 25, 2013 (138)
37 ILLUMINA ss778603686 Aug 21, 2014 (142)
38 ILLUMINA ss783235696 Sep 08, 2015 (146)
39 ILLUMINA ss784189706 Aug 21, 2014 (142)
40 ILLUMINA ss832496190 Sep 08, 2015 (146)
41 ILLUMINA ss834061004 Aug 21, 2014 (142)
42 EVA-GONL ss975890017 Aug 21, 2014 (142)
43 JMKIDD_LAB ss1068420628 Aug 21, 2014 (142)
44 1000GENOMES ss1293715901 Aug 21, 2014 (142)
45 DDI ss1426039326 Apr 01, 2015 (144)
46 EVA_GENOME_DK ss1574524235 Apr 01, 2015 (144)
47 EVA_DECODE ss1585281485 Apr 01, 2015 (144)
48 EVA_UK10K_ALSPAC ss1601637891 Apr 01, 2015 (144)
49 EVA_UK10K_TWINSUK ss1644631924 Apr 01, 2015 (144)
50 EVA_MGP ss1710935459 Apr 01, 2015 (144)
51 EVA_SVP ss1712387210 Apr 01, 2015 (144)
52 ILLUMINA ss1751885579 Sep 08, 2015 (146)
53 WEILL_CORNELL_DGM ss1919125738 Feb 12, 2016 (147)
54 GENOMED ss1966915160 Jul 19, 2016 (147)
55 JJLAB ss2020079556 Sep 14, 2016 (149)
56 USC_VALOUEV ss2148107467 Dec 20, 2016 (150)
57 HUMAN_LONGEVITY ss2168156444 Dec 20, 2016 (150)
58 SYSTEMSBIOZJU ss2624548065 Nov 08, 2017 (151)
59 ILLUMINA ss2632601762 Nov 08, 2017 (151)
60 GRF ss2698089342 Nov 08, 2017 (151)
61 ILLUMINA ss2710687687 Nov 08, 2017 (151)
62 GNOMAD ss2763552543 Nov 08, 2017 (151)
63 SWEGEN ss2988069099 Nov 08, 2017 (151)
64 BIOINF_KMB_FNS_UNIBA ss3023799427 Nov 08, 2017 (151)
65 CSHL ss3343803287 Nov 08, 2017 (151)
66 ILLUMINA ss3626257003 Oct 11, 2018 (152)
67 ILLUMINA ss3630633115 Oct 11, 2018 (152)
68 ILLUMINA ss3632917681 Oct 11, 2018 (152)
69 ILLUMINA ss3633613363 Oct 11, 2018 (152)
70 ILLUMINA ss3634361859 Oct 11, 2018 (152)
71 ILLUMINA ss3635306648 Oct 11, 2018 (152)
72 ILLUMINA ss3636040736 Oct 11, 2018 (152)
73 ILLUMINA ss3637057161 Oct 11, 2018 (152)
74 ILLUMINA ss3637800506 Oct 11, 2018 (152)
75 ILLUMINA ss3640069213 Oct 11, 2018 (152)
76 ILLUMINA ss3642808371 Oct 11, 2018 (152)
77 OMUKHERJEE_ADBS ss3646249905 Oct 11, 2018 (152)
78 URBANLAB ss3646834435 Oct 11, 2018 (152)
79 EGCUT_WGS ss3656019135 Jul 12, 2019 (153)
80 EVA_DECODE ss3688167315 Jul 12, 2019 (153)
81 ACPOP ss3727657080 Jul 12, 2019 (153)
82 ILLUMINA ss3744662725 Jul 12, 2019 (153)
83 EVA ss3747049390 Jul 12, 2019 (153)
84 ILLUMINA ss3772163748 Jul 12, 2019 (153)
85 PACBIO ss3783623967 Jul 12, 2019 (153)
86 PACBIO ss3789246187 Jul 12, 2019 (153)
87 PACBIO ss3794118330 Jul 12, 2019 (153)
88 KHV_HUMAN_GENOMES ss3800050421 Jul 12, 2019 (153)
89 EVA ss3825582632 Apr 25, 2020 (154)
90 EVA ss3826526847 Apr 25, 2020 (154)
91 EVA ss3836659784 Apr 25, 2020 (154)
92 EVA ss3842070114 Apr 25, 2020 (154)
93 SGDP_PRJ ss3850411423 Apr 25, 2020 (154)
94 KRGDB ss3895672198 Apr 25, 2020 (154)
95 KOGIC ss3946040598 Apr 25, 2020 (154)
96 FSA-LAB ss3983956246 Apr 25, 2021 (155)
97 FSA-LAB ss3983956247 Apr 25, 2021 (155)
98 EVA ss3984838393 Apr 25, 2021 (155)
99 EVA ss3986014362 Apr 25, 2021 (155)
100 TOPMED ss4475266584 Apr 25, 2021 (155)
101 TOMMO_GENOMICS ss5147372036 Apr 25, 2021 (155)
102 1000G_HIGH_COVERAGE ss5244976357 Oct 12, 2022 (156)
103 EVA ss5314666031 Oct 12, 2022 (156)
104 EVA ss5323301659 Oct 12, 2022 (156)
105 HUGCELL_USP ss5445493751 Oct 12, 2022 (156)
106 EVA ss5506101713 Oct 12, 2022 (156)
107 1000G_HIGH_COVERAGE ss5518649251 Oct 12, 2022 (156)
108 SANFORD_IMAGENETICS ss5626981042 Oct 12, 2022 (156)
109 TOMMO_GENOMICS ss5674828019 Oct 12, 2022 (156)
110 EVA ss5799505149 Oct 12, 2022 (156)
111 YY_MCH ss5801430394 Oct 12, 2022 (156)
112 EVA ss5832936313 Oct 12, 2022 (156)
113 EVA ss5849186802 Oct 12, 2022 (156)
114 EVA ss5911034735 Oct 12, 2022 (156)
115 EVA ss5938796722 Oct 12, 2022 (156)
116 1000Genomes NC_000001.10 - 183114634 Oct 11, 2018 (152)
117 1000Genomes_30x NC_000001.11 - 183145499 Oct 12, 2022 (156)
118 The Avon Longitudinal Study of Parents and Children NC_000001.10 - 183114634 Oct 11, 2018 (152)
119 Genetic variation in the Estonian population NC_000001.10 - 183114634 Oct 11, 2018 (152)
120 The Danish reference pan genome NC_000001.10 - 183114634 Apr 25, 2020 (154)
121 gnomAD - Genomes NC_000001.11 - 183145499 Apr 25, 2021 (155)
122 Genome of the Netherlands Release 5 NC_000001.10 - 183114634 Apr 25, 2020 (154)
123 HapMap NC_000001.11 - 183145499 Apr 25, 2020 (154)
124 KOREAN population from KRGDB NC_000001.10 - 183114634 Apr 25, 2020 (154)
125 Korean Genome Project NC_000001.11 - 183145499 Apr 25, 2020 (154)
126 Medical Genome Project healthy controls from Spanish population NC_000001.10 - 183114634 Apr 25, 2020 (154)
127 Northern Sweden NC_000001.10 - 183114634 Jul 12, 2019 (153)
128 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000001.10 - 183114634 Apr 25, 2021 (155)
129 Qatari NC_000001.10 - 183114634 Apr 25, 2020 (154)
130 SGDP_PRJ NC_000001.10 - 183114634 Apr 25, 2020 (154)
131 Siberian NC_000001.10 - 183114634 Apr 25, 2020 (154)
132 8.3KJPN NC_000001.10 - 183114634 Apr 25, 2021 (155)
133 14KJPN NC_000001.11 - 183145499 Oct 12, 2022 (156)
134 TopMed NC_000001.11 - 183145499 Apr 25, 2021 (155)
135 UK 10K study - Twins NC_000001.10 - 183114634 Oct 11, 2018 (152)
136 A Vietnamese Genetic Variation Database NC_000001.10 - 183114634 Jul 12, 2019 (153)
137 ALFA NC_000001.11 - 183145499 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)
rs1065073 Dec 16, 2002 (110)
rs1537519 Jan 18, 2001 (92)
rs3206099 Jul 03, 2002 (106)
rs3738826 Oct 09, 2002 (108)
rs386610462 Aug 21, 2014 (142)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss87892934, ss108757795, ss111450413, ss164602958, ss165527817, ss167349025, ss199333775, ss205234450, ss253657738, ss276127318, ss290677666, ss481570398, ss1585281485, ss1712387210, ss3642808371 NC_000001.9:181381256:G:A NC_000001.11:183145498:G:A (self)
4535702, 2486537, 1757383, 1789330, 1080096, 2849592, 52211, 941945, 64320, 1167668, 2428403, 623821, 5341343, 2486537, 532778, ss218757215, ss230810192, ss238440401, ss481600171, ss482571819, ss485580242, ss537473483, ss648544752, ss778603686, ss783235696, ss784189706, ss832496190, ss834061004, ss975890017, ss1068420628, ss1293715901, ss1426039326, ss1574524235, ss1601637891, ss1644631924, ss1710935459, ss1751885579, ss1919125738, ss1966915160, ss2020079556, ss2148107467, ss2624548065, ss2632601762, ss2698089342, ss2710687687, ss2763552543, ss2988069099, ss3343803287, ss3626257003, ss3630633115, ss3632917681, ss3633613363, ss3634361859, ss3635306648, ss3636040736, ss3637057161, ss3637800506, ss3640069213, ss3646249905, ss3656019135, ss3727657080, ss3744662725, ss3747049390, ss3772163748, ss3783623967, ss3789246187, ss3794118330, ss3825582632, ss3826526847, ss3836659784, ss3850411423, ss3895672198, ss3983956246, ss3983956247, ss3984838393, ss3986014362, ss5147372036, ss5314666031, ss5323301659, ss5506101713, ss5626981042, ss5799505149, ss5832936313, ss5938796722 NC_000001.10:183114633:G:A NC_000001.11:183145498:G:A (self)
6175186, 32742326, 218456, 2418599, 8665123, 38872919, 7579303324, ss2168156444, ss3023799427, ss3646834435, ss3688167315, ss3800050421, ss3842070114, ss3946040598, ss4475266584, ss5244976357, ss5445493751, ss5518649251, ss5674828019, ss5801430394, ss5849186802, ss5911034735 NC_000001.11:183145498:G:A NC_000001.11:183145498:G:A (self)
ss16400450, ss20582382 NT_004487.16:12163130:G:A NC_000001.11:183145498:G:A (self)
ss1554741, ss2379006, ss4436131, ss4924826, ss23853351, ss43869276, ss65739652, ss74856631, ss102643995, ss138116111, ss144237558, ss156005571, ss160880942, ss174379922 NT_004487.19:34603275:G:A NC_000001.11:183145498:G:A (self)
7579303324 NC_000001.11:183145498:G:T NC_000001.11:183145498:G:T (self)
Help

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

2 citations for rs7473
PMID Title Author Year Journal
33073494 An in silico approach to identify and prioritize miRNAs target sites polymorphisms in colorectal cancer and obesity. Gholami M et al. 2020 Cancer medicine
35373932 Association of miRNA targetome variants in LAMC1 and GNB3 genes with colorectal cancer and obesity. Gholami M et al. 2022 Cancer medicine
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