rs10995170
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10995170(C;C) |
| Make rs10995170(C;T) |
| Make rs10995170(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 62463624 |
| Gene | ZNF365 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10995170 |
| dbSNP (classic) | rs10995170 |
| ClinGen | rs10995170 |
| ebi | rs10995170 |
| HLI | rs10995170 |
| Exac | rs10995170 |
| Gnomad | rs10995170 |
| Varsome | rs10995170 |
| LitVar | rs10995170 |
| Map | rs10995170 |
| PheGenI | rs10995170 |
| Biobank | rs10995170 |
| 1000 genomes | rs10995170 |
| hgdp | rs10995170 |
| ensembl | rs10995170 |
| geneview | rs10995170 |
| scholar | rs10995170 |
| rs10995170 | |
| pharmgkb | rs10995170 |
| gwascentral | rs10995170 |
| openSNP | rs10995170 |
| 23andMe | rs10995170 |
| SNPshot | rs10995170 |
| SNPdbe | rs10995170 |
| MSV3d | rs10995170 |
| GWAS Ctlg | rs10995170 |
| GMAF | 0.2989 |
| 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 | 3E-7 |
| Odds Ratio | 4.4200 None |
