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rs869025469

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869025469(A;C)
Make rs869025469(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position47332975
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs869025469
ebirs869025469
HLIrs869025469
Exacrs869025469
Varsomers869025469
Maprs869025469
PheGenIrs869025469
hapmaprs869025469
1000 genomesrs869025469
hgdprs869025469
ensemblrs869025469
gopubmedrs869025469
geneviewrs869025469
scholarrs869025469
googlers869025469
pharmgkbrs869025469
gwascentralrs869025469
openSNPrs869025469
23andMers869025469
23andMe allrs869025469
SNP Nexus

SNPshotrs869025469
SNPdbers869025469
MSV3drs869025469
GWAS Ctlgrs869025469
Max Magnitude0
ClinVar
Risk rs869025469(C;C)
Alt rs869025469(C;C)
Reference rs869025469(A;A)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47354526T>G
CLNSRC
CLNACC RCV000208403.1,