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rs863225112

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225112(A;A)
Make rs863225112(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position47337727
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs863225112
ebirs863225112
HLIrs863225112
Exacrs863225112
Varsomers863225112
Maprs863225112
PheGenIrs863225112
hapmaprs863225112
1000 genomesrs863225112
hgdprs863225112
ensemblrs863225112
gopubmedrs863225112
geneviewrs863225112
scholarrs863225112
googlers863225112
pharmgkbrs863225112
gwascentralrs863225112
openSNPrs863225112
23andMers863225112
23andMe allrs863225112
SNP Nexus

SNPshotrs863225112
SNPdbers863225112
MSV3drs863225112
GWAS Ctlgrs863225112
Max Magnitude0
ClinVar
Risk rs863225112(A;A)
Alt rs863225112(A;A)
Reference rs863225112(G;G)
Significance Probable-Pathogenic
Disease Familial hypertrophic cardiomyopathy 4
Variation info
Gene MYBPC3
CLNDBN Familial hypertrophic cardiomyopathy 4
Reversed 1
HGVS NC_000011.9:g.47359278C>T
CLNSRC
CLNACC RCV000201451.1,