rs3729931

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs3729931(C;T)

Make rs3729931(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

12585017

Gene

RAF1

is a	snp
is	mentioned by
dbSNP	rs3729931
dbSNP (classic)	rs3729931
ClinGen	rs3729931
ebi	rs3729931
HLI	rs3729931
Exac	rs3729931
Gnomad	rs3729931
Varsome	rs3729931
LitVar	rs3729931
Map	rs3729931
PheGenI	rs3729931
Biobank	rs3729931
1000 genomes	rs3729931
hgdp	rs3729931
ensembl	rs3729931
geneview	rs3729931
scholar	rs3729931
google	rs3729931
pharmgkb	rs3729931
gwascentral	rs3729931
openSNP	rs3729931
23andMe	rs3729931
SNPshot	rs3729931
SNPdbe	rs3729931
MSV3d	rs3729931
GWAS Ctlg	rs3729931

GMAF

0.3815

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 21348951]
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,