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rs869025466

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025466(A;A)
Make rs869025466(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position47342157
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs869025466
ebirs869025466
HLIrs869025466
Exacrs869025466
Varsomers869025466
Maprs869025466
PheGenIrs869025466
hapmaprs869025466
1000 genomesrs869025466
hgdprs869025466
ensemblrs869025466
gopubmedrs869025466
geneviewrs869025466
scholarrs869025466
googlers869025466
pharmgkbrs869025466
gwascentralrs869025466
openSNPrs869025466
23andMers869025466
23andMe allrs869025466
SNP Nexus

SNPshotrs869025466
SNPdbers869025466
MSV3drs869025466
GWAS Ctlgrs869025466
Max Magnitude0
ClinVar
Risk rs869025466(A;A)
Alt rs869025466(A;A)
Reference rs869025466(G;G)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47363708C>T
CLNSRC
CLNACC RCV000208396.1,