rs1079596
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1079596(A;A) |
| Make rs1079596(A;G) |
| Make rs1079596(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 113425897 |
| Gene | DRD2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1079596 |
| dbSNP (classic) | rs1079596 |
| ClinGen | rs1079596 |
| ebi | rs1079596 |
| HLI | rs1079596 |
| Exac | rs1079596 |
| Gnomad | rs1079596 |
| Varsome | rs1079596 |
| LitVar | rs1079596 |
| Map | rs1079596 |
| PheGenI | rs1079596 |
| Biobank | rs1079596 |
| 1000 genomes | rs1079596 |
| hgdp | rs1079596 |
| ensembl | rs1079596 |
| geneview | rs1079596 |
| scholar | rs1079596 |
| rs1079596 | |
| pharmgkb | rs1079596 |
| gwascentral | rs1079596 |
| openSNP | rs1079596 |
| 23andMe | rs1079596 |
| SNPshot | rs1079596 |
| SNPdbe | rs1079596 |
| MSV3d | rs1079596 |
| GWAS Ctlg | rs1079596 |
| GMAF | 0.2332 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 17903293 ]
|
| Trait | Select biomarker traits |
| Title | Genome-wide association with select biomarker traits in the Framingham Heart Study |
| Risk Allele | |
| P-val | 0.0000030000000000000001 |
| Odds Ratio | NR NR |
[PMID 18821566] SNPs in dopamine D2 receptor gene (DRD2) and norepinephrine transporter gene (NET) are associated with continuous performance task (CPT) phenotypes in ADHD children and their families.
[PMID 19968402] Evaluation of genetic variability in the dopamine receptor D2 in relation to behavioral inhibition and impulsivity/sensation seeking: an exploratory study with d-amphetamine in healthy participants.
