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rs863224899

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224899(A;A)
Make rs863224899(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position47337580
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs863224899
ebirs863224899
HLIrs863224899
Exacrs863224899
Varsomers863224899
Maprs863224899
PheGenIrs863224899
hapmaprs863224899
1000 genomesrs863224899
hgdprs863224899
ensemblrs863224899
gopubmedrs863224899
geneviewrs863224899
scholarrs863224899
googlers863224899
pharmgkbrs863224899
gwascentralrs863224899
openSNPrs863224899
23andMers863224899
23andMe allrs863224899
SNP Nexus

SNPshotrs863224899
SNPdbers863224899
MSV3drs863224899
GWAS Ctlgrs863224899
Max Magnitude0
ClinVar
Risk rs863224899(A;A)
Alt rs863224899(A;A)
Reference rs863224899(G;G)
Significance Probable-Pathogenic
Disease Dilated cardiomyopathy 1A Familial hypertrophic cardiomyopathy 4
Variation info
Gene MYBPC3
CLNDBN Dilated cardiomyopathy 1A Familial hypertrophic cardiomyopathy 4
Reversed 1
HGVS NC_000011.9:g.47359131C>T
CLNSRC
CLNACC RCV000200036.1,