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rs397516031

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516031(A;A)
Make rs397516031(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position47332565
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397516031
ebirs397516031
HLIrs397516031
Exacrs397516031
Varsomers397516031
Maprs397516031
PheGenIrs397516031
hapmaprs397516031
1000 genomesrs397516031
hgdprs397516031
ensemblrs397516031
gopubmedrs397516031
geneviewrs397516031
scholarrs397516031
googlers397516031
pharmgkbrs397516031
gwascentralrs397516031
openSNPrs397516031
23andMers397516031
23andMe allrs397516031
SNP Nexus

SNPshotrs397516031
SNPdbers397516031
MSV3drs397516031
GWAS Ctlgrs397516031
Max Magnitude0
ClinVar
Risk rs397516031(A;A)
Alt rs397516031(A;A)
Reference rs397516031(G;G)
Significance Pathogenic
Disease not provided Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN not provided Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47354116C>T
CLNSRC ClinVar
CLNACC RCV000158248.2, RCV000208235.2,