rs7792596
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7792596(C;C) |
| Make rs7792596(C;T) |
| Make rs7792596(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 94380322 |
| Gene | LOC101927525 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7792596 |
| dbSNP (classic) | rs7792596 |
| ClinGen | rs7792596 |
| ebi | rs7792596 |
| HLI | rs7792596 |
| Exac | rs7792596 |
| Gnomad | rs7792596 |
| Varsome | rs7792596 |
| LitVar | rs7792596 |
| Map | rs7792596 |
| PheGenI | rs7792596 |
| Biobank | rs7792596 |
| 1000 genomes | rs7792596 |
| hgdp | rs7792596 |
| ensembl | rs7792596 |
| geneview | rs7792596 |
| scholar | rs7792596 |
| rs7792596 | |
| pharmgkb | rs7792596 |
| gwascentral | rs7792596 |
| openSNP | rs7792596 |
| 23andMe | rs7792596 |
| SNPshot | rs7792596 |
| SNPdbe | rs7792596 |
| MSV3d | rs7792596 |
| GWAS Ctlg | rs7792596 |
| GMAF | 0.388 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22449649] |
| Trait | |
| Title | Genome-wide association study of intelligence: additive effects of novel brain expressed genes. |
| Risk Allele | |
| P-val | 6E-7 |
| Odds Ratio | 4.1300 None |
