Have questions? Visit https://www.reddit.com/r/SNPedia

rs397515939

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515939(C;T)
Make rs397515939(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47339758
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397515939
ebirs397515939
HLIrs397515939
Exacrs397515939
Varsomers397515939
Maprs397515939
PheGenIrs397515939
hapmaprs397515939
1000 genomesrs397515939
hgdprs397515939
ensemblrs397515939
gopubmedrs397515939
geneviewrs397515939
scholarrs397515939
googlers397515939
pharmgkbrs397515939
gwascentralrs397515939
openSNPrs397515939
23andMers397515939
23andMe allrs397515939
SNP Nexus

SNPshotrs397515939
SNPdbers397515939
MSV3drs397515939
GWAS Ctlgrs397515939
Max Magnitude0
ClinVar
Risk rs397515939(G,T;G,T)
Alt rs397515939(G,T;G,T)
Reference rs397515939(C;C)
Significance Probable-Pathogenic
Disease not specified Primary dilated cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN not specified Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47361309G>A; NC_000011.9:g.47361309G>C
CLNSRC
CLNACC RCV000035455.4, RCV000157310.1,