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rs863225108

From SNPedia

Orientationminus
Geno Mag Summary
(AGA;AGA) 0 common in clinvar
Make rs863225108(-;-)
Make rs863225108(-;AAG)
Make rs863225108(AAG;AAG)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position47337560
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs863225108
ebirs863225108
HLIrs863225108
Exacrs863225108
Varsomers863225108
Maprs863225108
PheGenIrs863225108
hapmaprs863225108
1000 genomesrs863225108
hgdprs863225108
ensemblrs863225108
gopubmedrs863225108
geneviewrs863225108
scholarrs863225108
googlers863225108
pharmgkbrs863225108
gwascentralrs863225108
openSNPrs863225108
23andMers863225108
23andMe allrs863225108
SNP Nexus

SNPshotrs863225108
SNPdbers863225108
MSV3drs863225108
GWAS Ctlgrs863225108
Max Magnitude0
ClinVar
Risk rs863225108(;)
Alt rs863225108(;)
Reference rs863225108(AGA;AGA)
Significance Probable-Pathogenic
Disease not specified Primary familial hypertrophic cardiomyopathy Familial hypertrophic cardiomyopathy 4 Hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN not specified Primary familial hypertrophic cardiomyopathy Familial hypertrophic cardiomyopathy 4 Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47359101_47359103delTCT
CLNSRC
CLNACC RCV000154301.2, RCV000157327.2, RCV000168801.1, RCV000196806.2,