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rs397516028

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397516028(C;C)
Make rs397516028(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position47332594
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397516028
ebirs397516028
HLIrs397516028
Exacrs397516028
Varsomers397516028
Maprs397516028
PheGenIrs397516028
hapmaprs397516028
1000 genomesrs397516028
hgdprs397516028
ensemblrs397516028
gopubmedrs397516028
geneviewrs397516028
scholarrs397516028
googlers397516028
pharmgkbrs397516028
gwascentralrs397516028
openSNPrs397516028
23andMers397516028
23andMe allrs397516028
SNP Nexus

SNPshotrs397516028
SNPdbers397516028
MSV3drs397516028
GWAS Ctlgrs397516028
Max Magnitude0
ClinVar
Risk rs397516028(C;C)
Alt rs397516028(C;C)
Reference rs397516028(T;T)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy Familial hypertrophic cardiomyopathy 4
Variation info
Gene MYBPC3
CLNDBN Primary dilated cardiomyopathy Familial hypertrophic cardiomyopathy 4
Reversed 1
HGVS NC_000011.9:g.47354145A>G
CLNSRC ClinVar
CLNACC RCV000035600.2, RCV000201471.1,