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rs863225114

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863225114(-;C)
Make rs863225114(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position47332889
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs863225114
ClinGenrs863225114
ebirs863225114
HLIrs863225114
Exacrs863225114
Varsomers863225114
Maprs863225114
PheGenIrs863225114
hapmaprs863225114
1000 genomesrs863225114
hgdprs863225114
ensemblrs863225114
gopubmedrs863225114
geneviewrs863225114
scholarrs863225114
googlers863225114
pharmgkbrs863225114
gwascentralrs863225114
openSNPrs863225114
23andMers863225114
23andMe allrs863225114
SNP Nexus

SNPshotrs863225114
SNPdbers863225114
MSV3drs863225114
GWAS Ctlgrs863225114
Max Magnitude0
ClinVar
Risk rs863225114(C;C)
Alt rs863225114(C;C)
Reference Rs863225114(-;-)
Significance Probable-Pathogenic
Disease Familial hypertrophic cardiomyopathy 4
Variation info
Gene MYBPC3
CLNDBN Familial hypertrophic cardiomyopathy 4
Reversed 1
HGVS NC_000011.9:g.47354441dupG
CLNSRC
CLNACC RCV000201466.1,