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rs727503212

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503212(-;-)
Make rs727503212(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47347669
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs727503212
ebirs727503212
HLIrs727503212
Exacrs727503212
Varsomers727503212
Maprs727503212
PheGenIrs727503212
hapmaprs727503212
1000 genomesrs727503212
hgdprs727503212
ensemblrs727503212
gopubmedrs727503212
geneviewrs727503212
scholarrs727503212
googlers727503212
pharmgkbrs727503212
gwascentralrs727503212
openSNPrs727503212
23andMers727503212
23andMe allrs727503212
SNP Nexus

SNPshotrs727503212
SNPdbers727503212
MSV3drs727503212
GWAS Ctlgrs727503212
Max Magnitude0
ClinVar
Risk rs727503212(;)
Alt rs727503212(;)
Reference rs727503212(G;G)
Significance Other
Disease not provided Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN not provided Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47369220delC
CLNSRC
CLNACC RCV000158419.2, RCV000208471.2,