rs1375785
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1375785(A;A) |
| Make rs1375785(A;C) |
| Make rs1375785(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 83078996 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1375785 |
| dbSNP (classic) | rs1375785 |
| ClinGen | rs1375785 |
| ebi | rs1375785 |
| HLI | rs1375785 |
| Exac | rs1375785 |
| Gnomad | rs1375785 |
| Varsome | rs1375785 |
| LitVar | rs1375785 |
| Map | rs1375785 |
| PheGenI | rs1375785 |
| Biobank | rs1375785 |
| 1000 genomes | rs1375785 |
| hgdp | rs1375785 |
| ensembl | rs1375785 |
| geneview | rs1375785 |
| scholar | rs1375785 |
| rs1375785 | |
| pharmgkb | rs1375785 |
| gwascentral | rs1375785 |
| openSNP | rs1375785 |
| 23andMe | rs1375785 |
| SNPshot | rs1375785 |
| SNPdbe | rs1375785 |
| MSV3d | rs1375785 |
| GWAS Ctlg | rs1375785 |
| GMAF | 0.1607 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21130836 ]
|
| Trait | |
| Title | Whole genome association scan for genetic polymorphisms influencing information processing speed |
| Risk Allele | A |
| P-val | 0.000008 |
| Odds Ratio | 0.2000 [0.10-0.30] unit decrease |
