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rs397516068

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516068(C;C)
Make rs397516068(C;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position47348541
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397516068
ebirs397516068
HLIrs397516068
Exacrs397516068
Varsomers397516068
Maprs397516068
PheGenIrs397516068
hapmaprs397516068
1000 genomesrs397516068
hgdprs397516068
ensemblrs397516068
gopubmedrs397516068
geneviewrs397516068
scholarrs397516068
googlers397516068
pharmgkbrs397516068
gwascentralrs397516068
openSNPrs397516068
23andMers397516068
23andMe allrs397516068
SNP Nexus

SNPshotrs397516068
SNPdbers397516068
MSV3drs397516068
GWAS Ctlgrs397516068
Max Magnitude0
ClinVar
Risk rs397516068(C,T;C,T)
Alt rs397516068(C,T;C,T)
Reference rs397516068(G;G)
Significance Other
Disease Familial hypertrophic cardiomyopathy 4 Primary familial hypertrophic cardiomyopathy not provided Hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Familial hypertrophic cardiomyopathy 4 Primary familial hypertrophic cardiomyopathy not provided Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47370092C>A; NC_000011.9:g.47370092C>G
CLNSRC ClinVar
CLNACC RCV000168751.1, RCV000035660.3, RCV000158303.2, RCV000232070.1,