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rs397515982

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515982(A;A)
Make rs397515982(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position47335944
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397515982
ebirs397515982
HLIrs397515982
Exacrs397515982
Varsomers397515982
Maprs397515982
PheGenIrs397515982
hapmaprs397515982
1000 genomesrs397515982
hgdprs397515982
ensemblrs397515982
gopubmedrs397515982
geneviewrs397515982
scholarrs397515982
googlers397515982
pharmgkbrs397515982
gwascentralrs397515982
openSNPrs397515982
23andMers397515982
23andMe allrs397515982
SNP Nexus

SNPshotrs397515982
SNPdbers397515982
MSV3drs397515982
GWAS Ctlgrs397515982
Max Magnitude0
ClinVar
Risk rs397515982(A;A)
Alt rs397515982(A;A)
Reference rs397515982(G;G)
Significance Other
Disease Primary familial hypertrophic cardiomyopathy not provided Hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy not provided Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47357495C>T
CLNSRC ClinVar
CLNACC RCV000035519.3, RCV000158180.2, RCV000197345.2,