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rs397515926

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397515926(-;-)
Make rs397515926(-;A)
ReferenceGRCh38 38.1/141
Chromosome11
Position47341235
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397515926
ebirs397515926
HLIrs397515926
Exacrs397515926
Varsomers397515926
Maprs397515926
PheGenIrs397515926
hapmaprs397515926
1000 genomesrs397515926
hgdprs397515926
ensemblrs397515926
gopubmedrs397515926
geneviewrs397515926
scholarrs397515926
googlers397515926
pharmgkbrs397515926
gwascentralrs397515926
openSNPrs397515926
23andMers397515926
23andMe allrs397515926
SNP Nexus

SNPshotrs397515926
SNPdbers397515926
MSV3drs397515926
GWAS Ctlgrs397515926
Max Magnitude0
ClinVar
Risk rs397515926(;)
Alt rs397515926(;)
Reference rs397515926(A;A)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy not provided
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy not provided
Reversed 1
HGVS NC_000011.9:g.47362786delT
CLNSRC ClinVar
CLNACC RCV000035435.2, RCV000158353.2,