rs4861096
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4861096(C;C) |
| Make rs4861096(C;T) |
| Make rs4861096(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 41282694 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4861096 |
| dbSNP (classic) | rs4861096 |
| ClinGen | rs4861096 |
| ebi | rs4861096 |
| HLI | rs4861096 |
| Exac | rs4861096 |
| Gnomad | rs4861096 |
| Varsome | rs4861096 |
| LitVar | rs4861096 |
| Map | rs4861096 |
| PheGenI | rs4861096 |
| Biobank | rs4861096 |
| 1000 genomes | rs4861096 |
| hgdp | rs4861096 |
| ensembl | rs4861096 |
| geneview | rs4861096 |
| scholar | rs4861096 |
| rs4861096 | |
| pharmgkb | rs4861096 |
| gwascentral | rs4861096 |
| openSNP | rs4861096 |
| 23andMe | rs4861096 |
| SNPshot | rs4861096 |
| SNPdbe | rs4861096 |
| MSV3d | rs4861096 |
| GWAS Ctlg | rs4861096 |
| GMAF | 0.2695 |
| Max Magnitude | 0 |
| ? | (C;C) (C;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 | 9E-6 |
| Odds Ratio | NR NR |
