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

rs397515938

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515938(C;T)
Make rs397515938(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47339784
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397515938
ebirs397515938
HLIrs397515938
Exacrs397515938
Varsomers397515938
Maprs397515938
PheGenIrs397515938
hapmaprs397515938
1000 genomesrs397515938
hgdprs397515938
ensemblrs397515938
gopubmedrs397515938
geneviewrs397515938
scholarrs397515938
googlers397515938
pharmgkbrs397515938
gwascentralrs397515938
openSNPrs397515938
23andMers397515938
23andMe allrs397515938
SNP Nexus

SNPshotrs397515938
SNPdbers397515938
MSV3drs397515938
GWAS Ctlgrs397515938
Max Magnitude0
ClinVar
Risk rs397515938(T;T)
Alt rs397515938(T;T)
Reference rs397515938(C;C)
Significance Probable-Pathogenic
Disease not specified not provided Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN not specified not provided Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47361335G>A
CLNSRC
CLNACC RCV000035454.2, RCV000158134.1, RCV000208032.1,