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

rs143816093

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs143816093(C;G)
Make rs143816093(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position53609531
GeneWDR72
is asnp
is mentioned by
dbSNPrs143816093
ebirs143816093
HLIrs143816093
Exacrs143816093
Varsomers143816093
Maprs143816093
PheGenIrs143816093
hapmaprs143816093
1000 genomesrs143816093
hgdprs143816093
ensemblrs143816093
gopubmedrs143816093
geneviewrs143816093
scholarrs143816093
googlers143816093
pharmgkbrs143816093
gwascentralrs143816093
openSNPrs143816093
23andMers143816093
23andMe allrs143816093
SNP Nexus

SNPshotrs143816093
SNPdbers143816093
MSV3drs143816093
GWAS Ctlgrs143816093
GMAF0.0004591
Max Magnitude0
ClinVar
Risk rs143816093(G,T;G,T)
Alt rs143816093(G,T;G,T)
Reference rs143816093(C;C)
Significance Pathogenic
Disease Amelogenesis imperfecta
Variation info
Gene WDR72
CLNDBN Amelogenesis imperfecta, hypomaturation type, IIA3
Reversed 0
HGVS NC_000015.9:g.53901728C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000256.3,