rs10038113
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10038113(C;C) |
| Make rs10038113(C;T) |
| Make rs10038113(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 25902233 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10038113 |
| dbSNP (classic) | rs10038113 |
| ClinGen | rs10038113 |
| ebi | rs10038113 |
| HLI | rs10038113 |
| Exac | rs10038113 |
| Gnomad | rs10038113 |
| Varsome | rs10038113 |
| LitVar | rs10038113 |
| Map | rs10038113 |
| PheGenI | rs10038113 |
| Biobank | rs10038113 |
| 1000 genomes | rs10038113 |
| hgdp | rs10038113 |
| ensembl | rs10038113 |
| geneview | rs10038113 |
| scholar | rs10038113 |
| rs10038113 | |
| pharmgkb | rs10038113 |
| gwascentral | rs10038113 |
| openSNP | rs10038113 |
| 23andMe | rs10038113 |
| SNPshot | rs10038113 |
| SNPdbe | rs10038113 |
| MSV3d | rs10038113 |
| GWAS Ctlg | rs10038113 |
| GMAF | 0.4885 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19456320 ]
|
| Trait | Autism |
| Title | A genome-wide association study of autism reveals a common novel risk locus at 5p14.1 |
| Risk Allele | T |
| P-val | 0.000003 |
| Odds Ratio | 1.33 [1.11-1.43] |
