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rs869025460

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869025460(-;-)
Make rs869025460(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position47339375
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs869025460
ebirs869025460
HLIrs869025460
Exacrs869025460
Varsomers869025460
Maprs869025460
PheGenIrs869025460
hapmaprs869025460
1000 genomesrs869025460
hgdprs869025460
ensemblrs869025460
gopubmedrs869025460
geneviewrs869025460
scholarrs869025460
googlers869025460
pharmgkbrs869025460
gwascentralrs869025460
openSNPrs869025460
23andMers869025460
23andMe allrs869025460
SNP Nexus

SNPshotrs869025460
SNPdbers869025460
MSV3drs869025460
GWAS Ctlgrs869025460
Max Magnitude0
ClinVar
Risk rs869025460(;)
Alt rs869025460(;)
Reference rs869025460(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.47360926delT
CLNSRC
CLNACC RCV000208342.1,