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rs863225113

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225113(A;A)
Make rs863225113(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position47333224
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs863225113
ebirs863225113
HLIrs863225113
Exacrs863225113
Varsomers863225113
Maprs863225113
PheGenIrs863225113
hapmaprs863225113
1000 genomesrs863225113
hgdprs863225113
ensemblrs863225113
gopubmedrs863225113
geneviewrs863225113
scholarrs863225113
googlers863225113
pharmgkbrs863225113
gwascentralrs863225113
openSNPrs863225113
23andMers863225113
23andMe allrs863225113
SNP Nexus

SNPshotrs863225113
SNPdbers863225113
MSV3drs863225113
GWAS Ctlgrs863225113
Max Magnitude0
ClinVar
Risk rs863225113(A;A)
Alt rs863225113(A;A)
Reference Rs863225113(C;C)
Significance Probable-Pathogenic
Disease Familial hypertrophic cardiomyopathy 4
Variation info
Gene MYBPC3
CLNDBN Familial hypertrophic cardiomyopathy 4
Reversed 1
HGVS NC_000011.9:g.47354775G>T
CLNSRC
CLNACC RCV000201482.1,