Have questions? Visit https://www.reddit.com/r/SNPedia

rs863225104

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863225104(-;G)
Make rs863225104(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position47335943
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs863225104
ClinGenrs863225104
ebirs863225104
HLIrs863225104
Exacrs863225104
Varsomers863225104
Maprs863225104
PheGenIrs863225104
hapmaprs863225104
1000 genomesrs863225104
hgdprs863225104
ensemblrs863225104
gopubmedrs863225104
geneviewrs863225104
scholarrs863225104
googlers863225104
pharmgkbrs863225104
gwascentralrs863225104
openSNPrs863225104
23andMers863225104
23andMe allrs863225104
SNP Nexus

SNPshotrs863225104
SNPdbers863225104
MSV3drs863225104
GWAS Ctlgrs863225104
Max Magnitude0
ClinVar
Risk rs863225104(G;G)
Alt rs863225104(G;G)
Reference Rs863225104(;)
Significance Probable-Pathogenic
Disease Familial hypertrophic cardiomyopathy 4
Variation info
Gene MYBPC3
CLNDBN Familial hypertrophic cardiomyopathy 4
Reversed 1
HGVS NC_000011.9:g.47357495dupC
CLNSRC
CLNACC RCV000201439.1,