rs790356
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs790356(A;A) |
Make rs790356(A;G) |
Make rs790356(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 83909744 |
Gene | DLG2 |
is a | snp |
is | mentioned by |
dbSNP | rs790356 |
dbSNP (classic) | rs790356 |
ClinGen | rs790356 |
ebi | rs790356 |
HLI | rs790356 |
Exac | rs790356 |
Gnomad | rs790356 |
Varsome | rs790356 |
LitVar | rs790356 |
Map | rs790356 |
PheGenI | rs790356 |
Biobank | rs790356 |
1000 genomes | rs790356 |
hgdp | rs790356 |
ensembl | rs790356 |
geneview | rs790356 |
scholar | rs790356 |
rs790356 | |
pharmgkb | rs790356 |
gwascentral | rs790356 |
openSNP | rs790356 |
23andMe | rs790356 |
SNPshot | rs790356 |
SNPdbe | rs790356 |
MSV3d | rs790356 |
GWAS Ctlg | rs790356 |
GMAF | 0.3898 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22544364] |
Trait | |
Title | A genome-wide association study identifies susceptibility loci for Wilms tumor. |
Risk Allele | G |
P-val | 4E-15 |
Odds Ratio | 1.2800 None |