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rs397515991

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515991(A;A)
Make rs397515991(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position47335041
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397515991
ebirs397515991
HLIrs397515991
Exacrs397515991
Varsomers397515991
Maprs397515991
PheGenIrs397515991
hapmaprs397515991
1000 genomesrs397515991
hgdprs397515991
ensemblrs397515991
gopubmedrs397515991
geneviewrs397515991
scholarrs397515991
googlers397515991
pharmgkbrs397515991
gwascentralrs397515991
openSNPrs397515991
23andMers397515991
23andMe allrs397515991
SNP Nexus

SNPshotrs397515991
SNPdbers397515991
MSV3drs397515991
GWAS Ctlgrs397515991
Max Magnitude0
ClinVar
Risk rs397515991(A,C;A,C)
Alt rs397515991(A,C;A,C)
Reference rs397515991(G;G)
Significance Other
Disease Primary familial hypertrophic cardiomyopathy Familial hypertrophic cardiomyopathy 4 not provided Hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy Familial hypertrophic cardiomyopathy 4 not provided Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47356592C>G; NC_000011.9:g.47356592C>T
CLNSRC ClinVar
CLNACC RCV000035538.2, RCV000035537.5, RCV000158196.2, RCV000195678.2, RCV000211811.1,