rs1891498
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1891498(C;C) |
| Make rs1891498(C;T) |
| Make rs1891498(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 147754660 |
| Gene | LOC102723321 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1891498 |
| dbSNP (classic) | rs1891498 |
| ClinGen | rs1891498 |
| ebi | rs1891498 |
| HLI | rs1891498 |
| Exac | rs1891498 |
| Gnomad | rs1891498 |
| Varsome | rs1891498 |
| LitVar | rs1891498 |
| Map | rs1891498 |
| PheGenI | rs1891498 |
| Biobank | rs1891498 |
| 1000 genomes | rs1891498 |
| hgdp | rs1891498 |
| ensembl | rs1891498 |
| geneview | rs1891498 |
| scholar | rs1891498 |
| rs1891498 | |
| pharmgkb | rs1891498 |
| gwascentral | rs1891498 |
| openSNP | rs1891498 |
| 23andMe | rs1891498 |
| SNPshot | rs1891498 |
| SNPdbe | rs1891498 |
| MSV3d | rs1891498 |
| GWAS Ctlg | rs1891498 |
| GMAF | 0.1309 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20125193 ]
|
| Trait | Cognitive performance |
| Title | Common genetic variation and performance on standardized cognitive tests. |
| Risk Allele | |
| P-val | 9E-6 |
| Odds Ratio | NR NR |
