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rs587777587

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777587(A;A)
Make rs587777587(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position12584539
GeneRAF1
is asnp
is mentioned by
dbSNPrs587777587
ebirs587777587
HLIrs587777587
Exacrs587777587
Varsomers587777587
Maprs587777587
PheGenIrs587777587
hapmaprs587777587
1000 genomesrs587777587
hgdprs587777587
ensemblrs587777587
gopubmedrs587777587
geneviewrs587777587
scholarrs587777587
googlers587777587
pharmgkbrs587777587
gwascentralrs587777587
openSNPrs587777587
23andMers587777587
23andMe allrs587777587
SNP Nexus

SNPshotrs587777587
SNPdbers587777587
MSV3drs587777587
GWAS Ctlgrs587777587
Max Magnitude0
ClinVar
Risk rs587777587(A;A)
Alt rs587777587(A;A)
Reference rs587777587(G;G)
Significance Pathogenic
Disease Cardiomyopathy
Variation info
Gene RAF1
CLNDBN Cardiomyopathy, dilated, 1NN
Reversed 0
HGVS NC_000003.11:g.12626038G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000131336.3,