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rs869025501

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869025501(C;T)
Make rs869025501(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position12604191
GeneRAF1
is asnp
is mentioned by
dbSNPrs869025501
ebirs869025501
HLIrs869025501
Exacrs869025501
Varsomers869025501
Maprs869025501
PheGenIrs869025501
hapmaprs869025501
1000 genomesrs869025501
hgdprs869025501
ensemblrs869025501
gopubmedrs869025501
geneviewrs869025501
scholarrs869025501
googlers869025501
pharmgkbrs869025501
gwascentralrs869025501
openSNPrs869025501
23andMers869025501
23andMe allrs869025501
SNP Nexus

SNPshotrs869025501
SNPdbers869025501
MSV3drs869025501
GWAS Ctlgrs869025501
Max Magnitude0
ClinVar
Risk rs869025501(T;T)
Alt rs869025501(T;T)
Reference rs869025501(C;C)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene RAF1
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000003.11:g.12645690G>A
CLNSRC
CLNACC RCV000208050.1,