rs6486986
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6486986(G;G) |
| Make rs6486986(G;T) |
| Make rs6486986(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 19648661 |
| Gene | LOC101928387 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6486986 |
| dbSNP (classic) | rs6486986 |
| ClinGen | rs6486986 |
| ebi | rs6486986 |
| HLI | rs6486986 |
| Exac | rs6486986 |
| Gnomad | rs6486986 |
| Varsome | rs6486986 |
| LitVar | rs6486986 |
| Map | rs6486986 |
| PheGenI | rs6486986 |
| Biobank | rs6486986 |
| 1000 genomes | rs6486986 |
| hgdp | rs6486986 |
| ensembl | rs6486986 |
| geneview | rs6486986 |
| scholar | rs6486986 |
| rs6486986 | |
| pharmgkb | rs6486986 |
| gwascentral | rs6486986 |
| openSNP | rs6486986 |
| 23andMe | rs6486986 |
| SNPshot | rs6486986 |
| SNPdbe | rs6486986 |
| MSV3d | rs6486986 |
| GWAS Ctlg | rs6486986 |
| GMAF | 0.2378 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19734545 ]
|
| Trait | Cognitive performance |
| Title | A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. |
| Risk Allele | |
| P-val | 8E-6 |
| Odds Ratio | NR NR |
