rs9890413
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9890413(A;A) |
Make rs9890413(A;G) |
Make rs9890413(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 17 |
Position | 46824083 |
is a | snp |
is | mentioned by |
dbSNP | rs9890413 |
dbSNP (classic) | rs9890413 |
ClinGen | rs9890413 |
ebi | rs9890413 |
HLI | rs9890413 |
Exac | rs9890413 |
Gnomad | rs9890413 |
Varsome | rs9890413 |
LitVar | rs9890413 |
Map | rs9890413 |
PheGenI | rs9890413 |
Biobank | rs9890413 |
1000 genomes | rs9890413 |
hgdp | rs9890413 |
ensembl | rs9890413 |
geneview | rs9890413 |
scholar | rs9890413 |
rs9890413 | |
pharmgkb | rs9890413 |
gwascentral | rs9890413 |
openSNP | rs9890413 |
23andMe | rs9890413 |
SNPshot | rs9890413 |
SNPdbe | rs9890413 |
MSV3d | rs9890413 |
GWAS Ctlg | rs9890413 |
Max Magnitude | 0 |
[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