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rs587777588

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777588(C;T)
Make rs587777588(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position12604261
GeneRAF1
is asnp
is mentioned by
dbSNPrs587777588
ebirs587777588
HLIrs587777588
Exacrs587777588
Varsomers587777588
Maprs587777588
PheGenIrs587777588
hapmaprs587777588
1000 genomesrs587777588
hgdprs587777588
ensemblrs587777588
gopubmedrs587777588
geneviewrs587777588
scholarrs587777588
googlers587777588
pharmgkbrs587777588
gwascentralrs587777588
openSNPrs587777588
23andMers587777588
23andMe allrs587777588
SNP Nexus

SNPshotrs587777588
SNPdbers587777588
MSV3drs587777588
GWAS Ctlgrs587777588
Max Magnitude0
ClinVar
Risk rs587777588(T;T)
Alt rs587777588(T;T)
Reference rs587777588(C;C)
Significance Pathogenic
Disease Cardiomyopathy
Variation info
Gene RAF1
CLNDBN Cardiomyopathy, dilated, 1NN
Reversed 0
HGVS NC_000003.11:g.12645760C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000131337.3,