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rs9890413

From SNPedia

Orientationplus
Stabilizedplus
Make rs9890413(A;A)
Make rs9890413(A;G)
Make rs9890413(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position46824083
is asnp
is mentioned by
dbSNPrs9890413
dbSNP (classic)rs9890413
ClinGenrs9890413
ebirs9890413
HLIrs9890413
Exacrs9890413
Gnomadrs9890413
Varsomers9890413
LitVarrs9890413
Maprs9890413
PheGenIrs9890413
Biobankrs9890413
1000 genomesrs9890413
hgdprs9890413
ensemblrs9890413
geneviewrs9890413
scholarrs9890413
googlers9890413
pharmgkbrs9890413
gwascentralrs9890413
openSNPrs9890413
23andMers9890413
SNPshotrs9890413
SNPdbers9890413
MSV3drs9890413
GWAS Ctlgrs9890413
Max Magnitude0

[PMID 26505415] Variations in WNT3 gene are associated with incidence of non-syndromic cleft lip with or without cleft palate in a northeast Chinese population