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rs587777586

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587777586(A;G)
Make rs587777586(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position12584653
GeneRAF1
is asnp
is mentioned by
dbSNPrs587777586
ebirs587777586
HLIrs587777586
Exacrs587777586
Varsomers587777586
Maprs587777586
PheGenIrs587777586
hapmaprs587777586
1000 genomesrs587777586
hgdprs587777586
ensemblrs587777586
gopubmedrs587777586
geneviewrs587777586
scholarrs587777586
googlers587777586
pharmgkbrs587777586
gwascentralrs587777586
openSNPrs587777586
23andMers587777586
23andMe allrs587777586
SNP Nexus

SNPshotrs587777586
SNPdbers587777586
MSV3drs587777586
GWAS Ctlgrs587777586
Max Magnitude0
ClinVar
Risk rs587777586(A,G;A,G)
Alt rs587777586(A,G;A,G)
Reference rs587777586(T;T)
Significance Pathogenic
Disease Cardiomyopathy
Variation info
Gene RAF1
CLNDBN Cardiomyopathy, dilated, 1NN
Reversed 1
HGVS NC_000003.11:g.12626152A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000131334.3,