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rs869025464

From SNPedia

Orientationminus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs869025464(-;-)
Make rs869025464(-;TG)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position47350077
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs869025464
ebirs869025464
HLIrs869025464
Exacrs869025464
Varsomers869025464
Maprs869025464
PheGenIrs869025464
hapmaprs869025464
1000 genomesrs869025464
hgdprs869025464
ensemblrs869025464
gopubmedrs869025464
geneviewrs869025464
scholarrs869025464
googlers869025464
pharmgkbrs869025464
gwascentralrs869025464
openSNPrs869025464
23andMers869025464
23andMe allrs869025464
SNP Nexus

SNPshotrs869025464
SNPdbers869025464
MSV3drs869025464
GWAS Ctlgrs869025464
Max Magnitude0
ClinVar
Risk rs869025464(;)
Alt rs869025464(;)
Reference rs869025464(TG;TG)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47371628_47371629delCA
CLNSRC
CLNACC RCV000208286.1,