rs926938
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs926938(C;C) |
| Make rs926938(C;T) |
| Make rs926938(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 1 |
| Position | 114697195 |
| Gene | AMPD1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs926938 |
| dbSNP (classic) | rs926938 |
| ClinGen | rs926938 |
| ebi | rs926938 |
| HLI | rs926938 |
| Exac | rs926938 |
| Gnomad | rs926938 |
| Varsome | rs926938 |
| LitVar | rs926938 |
| Map | rs926938 |
| PheGenI | rs926938 |
| Biobank | rs926938 |
| 1000 genomes | rs926938 |
| hgdp | rs926938 |
| ensembl | rs926938 |
| geneview | rs926938 |
| scholar | rs926938 |
| rs926938 | |
| pharmgkb | rs926938 |
| gwascentral | rs926938 |
| openSNP | rs926938 |
| 23andMe | rs926938 |
| SNPshot | rs926938 |
| SNPdbe | rs926938 |
| MSV3d | rs926938 |
| GWAS Ctlg | rs926938 |
| Max Magnitude | 0 |
| GWAS snp | |
|---|---|
| PMID | [PMID 24189344] |
| Trait | Autism |
| Title | Common genetic variants on 1p13.2 associate with risk of autism. |
| Risk Allele | A |
| P-val | 4E-8 |
| Odds Ratio | 1.27 [NR] |
