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rs727503216

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727503216(C;T)
Make rs727503216(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47349871
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs727503216
ebirs727503216
HLIrs727503216
Exacrs727503216
Varsomers727503216
Maprs727503216
PheGenIrs727503216
hapmaprs727503216
1000 genomesrs727503216
hgdprs727503216
ensemblrs727503216
gopubmedrs727503216
geneviewrs727503216
scholarrs727503216
googlers727503216
pharmgkbrs727503216
gwascentralrs727503216
openSNPrs727503216
23andMers727503216
23andMe allrs727503216
SNP Nexus

SNPshotrs727503216
SNPdbers727503216
MSV3drs727503216
GWAS Ctlgrs727503216
Max Magnitude0
ClinVar
Risk rs727503216(T;T)
Alt rs727503216(T;T)
Reference rs727503216(C;C)
Significance Pathogenic
Disease not specified
Variation info
Gene MYBPC3
CLNDBN not specified
Reversed 1
HGVS NC_000011.9:g.47371422G>A
CLNSRC
CLNACC RCV000151163.1,