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rs863225110

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863225110(-;C)
Make rs863225110(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position47342931
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs863225110
ClinGenrs863225110
ebirs863225110
HLIrs863225110
Exacrs863225110
Varsomers863225110
Maprs863225110
PheGenIrs863225110
hapmaprs863225110
1000 genomesrs863225110
hgdprs863225110
ensemblrs863225110
gopubmedrs863225110
geneviewrs863225110
scholarrs863225110
googlers863225110
pharmgkbrs863225110
gwascentralrs863225110
openSNPrs863225110
23andMers863225110
23andMe allrs863225110
SNP Nexus

SNPshotrs863225110
SNPdbers863225110
MSV3drs863225110
GWAS Ctlgrs863225110
Max Magnitude0
ClinVar
Risk rs863225110(C;C)
Alt rs863225110(C;C)
Reference Rs863225110(;)
Significance Pathogenic
Disease Cardiomyopathy Familial hypertrophic cardiomyopathy 4
Variation info
Gene MYBPC3
CLNDBN Cardiomyopathy Familial hypertrophic cardiomyopathy 4
Reversed 1
HGVS NC_000011.9:g.47364480dupG
CLNSRC
CLNACC RCV000158474.1, RCV000201508.1,