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rs397516035

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397516035(A;T)
Make rs397516035(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position47332192
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397516035
ebirs397516035
HLIrs397516035
Exacrs397516035
Varsomers397516035
Maprs397516035
PheGenIrs397516035
hapmaprs397516035
1000 genomesrs397516035
hgdprs397516035
ensemblrs397516035
gopubmedrs397516035
geneviewrs397516035
scholarrs397516035
googlers397516035
pharmgkbrs397516035
gwascentralrs397516035
openSNPrs397516035
23andMers397516035
23andMe allrs397516035
SNP Nexus

SNPshotrs397516035
SNPdbers397516035
MSV3drs397516035
GWAS Ctlgrs397516035
Max Magnitude0
ClinVar
Risk rs397516035(T;T)
Alt rs397516035(T;T)
Reference rs397516035(A;A)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47353743T>A
CLNSRC ClinVar
CLNACC RCV000035608.2,