rs9879992
From SNPedia
Orientation | plus |
Make rs9879992(A;A) |
Make rs9879992(A;G) |
Make rs9879992(G;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 3 |
Position | 119993874 |
Gene | GSK3B |
is a | snp |
is | mentioned by |
dbSNP | rs9879992 |
dbSNP (classic) | rs9879992 |
ClinGen | rs9879992 |
ebi | rs9879992 |
HLI | rs9879992 |
Exac | rs9879992 |
Gnomad | rs9879992 |
Varsome | rs9879992 |
LitVar | rs9879992 |
Map | rs9879992 |
PheGenI | rs9879992 |
Biobank | rs9879992 |
1000 genomes | rs9879992 |
hgdp | rs9879992 |
ensembl | rs9879992 |
geneview | rs9879992 |
scholar | rs9879992 |
rs9879992 | |
pharmgkb | rs9879992 |
gwascentral | rs9879992 |
openSNP | rs9879992 |
23andMe | rs9879992 |
SNPshot | rs9879992 |
SNPdbe | rs9879992 |
MSV3d | rs9879992 |
GWAS Ctlg | rs9879992 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 30579133] Polymorphisms associated with oral clefts as potential susceptibility markers for oral and breast cancer.