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rs397515916

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397515916(A;T)
Make rs397515916(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position47342574
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397515916
ebirs397515916
HLIrs397515916
Exacrs397515916
Varsomers397515916
Maprs397515916
PheGenIrs397515916
hapmaprs397515916
1000 genomesrs397515916
hgdprs397515916
ensemblrs397515916
gopubmedrs397515916
geneviewrs397515916
scholarrs397515916
googlers397515916
pharmgkbrs397515916
gwascentralrs397515916
openSNPrs397515916
23andMers397515916
23andMe allrs397515916
SNP Nexus

SNPshotrs397515916
SNPdbers397515916
MSV3drs397515916
GWAS Ctlgrs397515916
Max Magnitude0
ClinVar
Risk rs397515916(T;T)
Alt rs397515916(T;T)
Reference rs397515916(A;A)
Significance Other
Disease Familial hypertrophic cardiomyopathy 4 not provided Hypertrophic cardiomyopathy Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Familial hypertrophic cardiomyopathy 4 not provided Hypertrophic cardiomyopathy Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47364125T>A
CLNSRC ClinVar
CLNACC RCV000035422.4, RCV000158106.2, RCV000168451.3, RCV000211799.1,