rs5016282
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs5016282(A;A) |
Make rs5016282(A;G) |
Make rs5016282(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 89008492 |
Gene | GRM5 |
is a | snp |
is | mentioned by |
dbSNP | rs5016282 |
dbSNP (classic) | rs5016282 |
ClinGen | rs5016282 |
ebi | rs5016282 |
HLI | rs5016282 |
Exac | rs5016282 |
Gnomad | rs5016282 |
Varsome | rs5016282 |
LitVar | rs5016282 |
Map | rs5016282 |
PheGenI | rs5016282 |
Biobank | rs5016282 |
1000 genomes | rs5016282 |
hgdp | rs5016282 |
ensembl | rs5016282 |
geneview | rs5016282 |
scholar | rs5016282 |
rs5016282 | |
pharmgkb | rs5016282 |
gwascentral | rs5016282 |
openSNP | rs5016282 |
23andMe | rs5016282 |
SNPshot | rs5016282 |
SNPdbe | rs5016282 |
MSV3d | rs5016282 |
GWAS Ctlg | rs5016282 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22012869] |
Trait | |
Title | Genome-wide association study in German patients with attention deficit/hyperactivity disorder. |
Risk Allele | A |
P-val | 0.000001 |
Odds Ratio | None None |