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rs397515888

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515888(G;T)
Make rs397515888(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position47343559
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397515888
ebirs397515888
HLIrs397515888
Exacrs397515888
Varsomers397515888
Maprs397515888
PheGenIrs397515888
hapmaprs397515888
1000 genomesrs397515888
hgdprs397515888
ensemblrs397515888
gopubmedrs397515888
geneviewrs397515888
scholarrs397515888
googlers397515888
pharmgkbrs397515888
gwascentralrs397515888
openSNPrs397515888
23andMers397515888
23andMe allrs397515888
SNP Nexus

SNPshotrs397515888
SNPdbers397515888
MSV3drs397515888
GWAS Ctlgrs397515888
Max Magnitude0
ClinVar
Risk rs397515888(T;T)
Alt rs397515888(T;T)
Reference rs397515888(G;G)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47365110C>A
CLNSRC ClinVar
CLNACC RCV000035372.2,