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rs397516082

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397516082(A;G)
Make rs397516082(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position47346372
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397516082
ebirs397516082
HLIrs397516082
Exacrs397516082
Varsomers397516082
Maprs397516082
PheGenIrs397516082
hapmaprs397516082
1000 genomesrs397516082
hgdprs397516082
ensemblrs397516082
gopubmedrs397516082
geneviewrs397516082
scholarrs397516082
googlers397516082
pharmgkbrs397516082
gwascentralrs397516082
openSNPrs397516082
23andMers397516082
23andMe allrs397516082
SNP Nexus

SNPshotrs397516082
SNPdbers397516082
MSV3drs397516082
GWAS Ctlgrs397516082
Max Magnitude0
ClinVar
Risk rs397516082(G;G)
Alt rs397516082(G;G)
Reference rs397516082(A;A)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy not provided
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy not provided
Reversed 1
HGVS NC_000011.9:g.47367923T>C
CLNSRC ClinVar
CLNACC RCV000035682.2, RCV000158322.2,