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rs397515920

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397515920(A;T)
Make rs397515920(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position47342088
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397515920
ebirs397515920
HLIrs397515920
Exacrs397515920
Varsomers397515920
Maprs397515920
PheGenIrs397515920
hapmaprs397515920
1000 genomesrs397515920
hgdprs397515920
ensemblrs397515920
gopubmedrs397515920
geneviewrs397515920
scholarrs397515920
googlers397515920
pharmgkbrs397515920
gwascentralrs397515920
openSNPrs397515920
23andMers397515920
23andMe allrs397515920
SNP Nexus

SNPshotrs397515920
SNPdbers397515920
MSV3drs397515920
GWAS Ctlgrs397515920
Max Magnitude0
ClinVar
Risk rs397515920(T;T)
Alt rs397515920(T;T)
Reference rs397515920(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.47363639T>A
CLNSRC ClinVar
CLNACC RCV000035427.2,