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rs397516010

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516010(G;T)
Make rs397516010(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position47333271
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397516010
ebirs397516010
HLIrs397516010
Exacrs397516010
Varsomers397516010
Maprs397516010
PheGenIrs397516010
hapmaprs397516010
1000 genomesrs397516010
hgdprs397516010
ensemblrs397516010
gopubmedrs397516010
geneviewrs397516010
scholarrs397516010
googlers397516010
pharmgkbrs397516010
gwascentralrs397516010
openSNPrs397516010
23andMers397516010
23andMe allrs397516010
SNP Nexus

SNPshotrs397516010
SNPdbers397516010
MSV3drs397516010
GWAS Ctlgrs397516010
Max Magnitude0
ClinVar
Risk rs397516010(C,T;C,T)
Alt rs397516010(C,T;C,T)
Reference rs397516010(G;G)
Significance Other
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47354822C>A
CLNSRC ClinVar
CLNACC RCV000208092.2,