rs71781329
From SNPedia
| Stabilized | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs71781329 |
| dbSNP (classic) | rs71781329 |
| ClinGen | rs71781329 |
| ebi | rs71781329 |
| HLI | rs71781329 |
| Exac | rs71781329 |
| Gnomad | rs71781329 |
| Varsome | rs71781329 |
| LitVar | rs71781329 |
| Map | rs71781329 |
| PheGenI | rs71781329 |
| Biobank | rs71781329 |
| 1000 genomes | rs71781329 |
| hgdp | rs71781329 |
| ensembl | rs71781329 |
| geneview | rs71781329 |
| scholar | rs71781329 |
| rs71781329 | |
| pharmgkb | rs71781329 |
| gwascentral | rs71781329 |
| openSNP | rs71781329 |
| 23andMe | rs71781329 |
| SNPshot | rs71781329 |
| SNPdbe | rs71781329 |
| MSV3d | rs71781329 |
| GWAS Ctlg | rs71781329 |
| Status | Deleted |
| Max Magnitude | 0 |
[PMID 25224256] Variants of the CNTNAP2 5' promoter as risk factors for autism spectrum disorders: a genetic and functional approach
