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rs3729931

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs3729931(C;T)
Make rs3729931(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position12585017
GeneRAF1
is asnp
is mentioned by
dbSNPrs3729931
ebirs3729931
HLIrs3729931
Exacrs3729931
Varsomers3729931
Maprs3729931
PheGenIrs3729931
hapmaprs3729931
1000 genomesrs3729931
hgdprs3729931
ensemblrs3729931
gopubmedrs3729931
geneviewrs3729931
scholarrs3729931
googlers3729931
pharmgkbrs3729931
gwascentralrs3729931
openSNPrs3729931
23andMers3729931
23andMe allrs3729931
SNP Nexus

SNPshotrs3729931
SNPdbers3729931
MSV3drs3729931
GWAS Ctlgrs3729931
GMAF0.3815
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21348951OA-icon.png]
Trait
Title Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality
Risk Allele
P-val 7E-7
Odds Ratio None None


ClinVar
Risk rs3729931(T;T)
Alt rs3729931(T;T)
Reference rs3729931(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene RAF1
CLNDBN not specified
Reversed 1
HGVS NC_000003.11:g.12626516G>A
CLNSRC ClinVar
CLNACC RCV000033615.5,