rs12690517
From SNPedia
| Merged into | rs1143674 |
| Orientation | plus |
| Stabilized | plus |
| Make rs12690517(A;A) |
| Make rs12690517(A;G) |
| Make rs12690517(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 181509807 |
| Gene | ITGA4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12690517 |
| dbSNP (classic) | rs12690517 |
| ClinGen | rs12690517 |
| ebi | rs12690517 |
| HLI | rs12690517 |
| Exac | rs12690517 |
| Gnomad | rs12690517 |
| Varsome | rs12690517 |
| LitVar | rs12690517 |
| Map | rs12690517 |
| PheGenI | rs12690517 |
| Biobank | rs12690517 |
| 1000 genomes | rs12690517 |
| hgdp | rs12690517 |
| ensembl | rs12690517 |
| geneview | rs12690517 |
| scholar | rs12690517 |
| rs12690517 | |
| pharmgkb | rs12690517 |
| gwascentral | rs12690517 |
| openSNP | rs12690517 |
| 23andMe | rs12690517 |
| SNPshot | rs12690517 |
| SNPdbe | rs12690517 |
| MSV3d | rs12690517 |
| GWAS Ctlg | rs12690517 |
| Status | Merged into rs1143674 |
| Max Magnitude | 0 |
[PMID 18846500] Fine mapping and association studies in a candidate region for autism on chromosome 2q31-q32
