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rs869025470

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869025470(C;C)
Make rs869025470(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position47332070
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs869025470
ebirs869025470
HLIrs869025470
Exacrs869025470
Varsomers869025470
Maprs869025470
PheGenIrs869025470
hapmaprs869025470
1000 genomesrs869025470
hgdprs869025470
ensemblrs869025470
gopubmedrs869025470
geneviewrs869025470
scholarrs869025470
googlers869025470
pharmgkbrs869025470
gwascentralrs869025470
openSNPrs869025470
23andMers869025470
23andMe allrs869025470
SNP Nexus

SNPshotrs869025470
SNPdbers869025470
MSV3drs869025470
GWAS Ctlgrs869025470
Max Magnitude0
ClinVar
Risk rs869025470(C;C)
Alt rs869025470(C;C)
Reference rs869025470(T;T)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47353621A>G
CLNSRC
CLNACC RCV000208425.1,