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rs6771157

From SNPedia

Orientationplus
Make rs6771157(C;C)
Make rs6771157(C;G)
Make rs6771157(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position38722372
GeneSCN10A
is asnp
is mentioned by
dbSNPrs6771157
ebirs6771157
HLIrs6771157
Exacrs6771157
Varsomers6771157
Maprs6771157
PheGenIrs6771157
hapmaprs6771157
1000 genomesrs6771157
hgdprs6771157
ensemblrs6771157
gopubmedrs6771157
geneviewrs6771157
scholarrs6771157
googlers6771157
pharmgkbrs6771157
gwascentralrs6771157
openSNPrs6771157
23andMers6771157
23andMe allrs6771157
SNP Nexus

SNPshotrs6771157
SNPdbers6771157
MSV3drs6771157
GWAS Ctlgrs6771157
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 27725708] The rs6771157 C/G polymorphism in SCN10A is associated with the risk of atrial fibrillation in a Chinese Han population.
ClinVar
Risk rs6771157(C;C)
Alt rs6771157(C;C)
Reference rs6771157(G;G)
Significance Non-pathogenic
Disease not specified
Variation info
Gene SCN10A
CLNDBN not specified
Reversed 0
HGVS NC_000003.11:g.38763863G>C
CLNSRC
CLNACC RCV000244131.1,