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rs869025463

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869025463(-;-)
Make rs869025463(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position47350551
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs869025463
ebirs869025463
HLIrs869025463
Exacrs869025463
Varsomers869025463
Maprs869025463
PheGenIrs869025463
hapmaprs869025463
1000 genomesrs869025463
hgdprs869025463
ensemblrs869025463
gopubmedrs869025463
geneviewrs869025463
scholarrs869025463
googlers869025463
pharmgkbrs869025463
gwascentralrs869025463
openSNPrs869025463
23andMers869025463
23andMe allrs869025463
SNP Nexus

SNPshotrs869025463
SNPdbers869025463
MSV3drs869025463
GWAS Ctlgrs869025463
Max Magnitude0
ClinVar
Risk rs869025463(;)
Alt rs869025463(;)
Reference rs869025463(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.47372102delT
CLNSRC
CLNACC RCV000208099.1,