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rs397515896

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397515896(-;-)
Make rs397515896(-;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position47343062
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397515896
ebirs397515896
HLIrs397515896
Exacrs397515896
Varsomers397515896
Maprs397515896
PheGenIrs397515896
hapmaprs397515896
1000 genomesrs397515896
hgdprs397515896
ensemblrs397515896
gopubmedrs397515896
geneviewrs397515896
scholarrs397515896
googlers397515896
pharmgkbrs397515896
gwascentralrs397515896
openSNPrs397515896
23andMers397515896
23andMe allrs397515896
SNP Nexus

SNPshotrs397515896
SNPdbers397515896
MSV3drs397515896
GWAS Ctlgrs397515896
Max Magnitude0
ClinVar
Risk rs397515896(;)
Alt rs397515896(;)
Reference rs397515896(T;T)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47364613delA
CLNSRC ClinVar
CLNACC RCV000035388.2,