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rs863225106

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225106(C;T)
Make rs863225106(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position47337732
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs863225106
ebirs863225106
HLIrs863225106
Exacrs863225106
Varsomers863225106
Maprs863225106
PheGenIrs863225106
hapmaprs863225106
1000 genomesrs863225106
hgdprs863225106
ensemblrs863225106
gopubmedrs863225106
geneviewrs863225106
scholarrs863225106
googlers863225106
pharmgkbrs863225106
gwascentralrs863225106
openSNPrs863225106
23andMers863225106
23andMe allrs863225106
SNP Nexus

SNPshotrs863225106
SNPdbers863225106
MSV3drs863225106
GWAS Ctlgrs863225106
Max Magnitude0
ClinVar
Risk rs863225106(T;T)
Alt rs863225106(T;T)
Reference rs863225106(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.47359283G>A
CLNSRC
CLNACC RCV000201498.1,