rs6538761
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6538761(A;A) |
| Make rs6538761(A;C) |
| Make rs6538761(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 97040442 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6538761 |
| dbSNP (classic) | rs6538761 |
| ClinGen | rs6538761 |
| ebi | rs6538761 |
| HLI | rs6538761 |
| Exac | rs6538761 |
| Gnomad | rs6538761 |
| Varsome | rs6538761 |
| LitVar | rs6538761 |
| Map | rs6538761 |
| PheGenI | rs6538761 |
| Biobank | rs6538761 |
| 1000 genomes | rs6538761 |
| hgdp | rs6538761 |
| ensembl | rs6538761 |
| geneview | rs6538761 |
| scholar | rs6538761 |
| rs6538761 | |
| pharmgkb | rs6538761 |
| gwascentral | rs6538761 |
| openSNP | rs6538761 |
| 23andMe | rs6538761 |
| SNPshot | rs6538761 |
| SNPdbe | rs6538761 |
| MSV3d | rs6538761 |
| GWAS Ctlg | rs6538761 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 24189344] |
| Trait | Autism |
| Title | Common genetic variants on 1p13.2 associate with risk of autism. |
| Risk Allele | A |
| P-val | 2E-6 |
| Odds Ratio | 1.24 [NR] |
