rs34712024
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs34712024(A;A) |
| Make rs34712024(A;G) |
| Make rs34712024(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 146116001 |
| Gene | CNTNAP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs34712024 |
| dbSNP (classic) | rs34712024 |
| ClinGen | rs34712024 |
| ebi | rs34712024 |
| HLI | rs34712024 |
| Exac | rs34712024 |
| Gnomad | rs34712024 |
| Varsome | rs34712024 |
| LitVar | rs34712024 |
| Map | rs34712024 |
| PheGenI | rs34712024 |
| Biobank | rs34712024 |
| 1000 genomes | rs34712024 |
| hgdp | rs34712024 |
| ensembl | rs34712024 |
| geneview | rs34712024 |
| scholar | rs34712024 |
| rs34712024 | |
| pharmgkb | rs34712024 |
| gwascentral | rs34712024 |
| openSNP | rs34712024 |
| 23andMe | rs34712024 |
| SNPshot | rs34712024 |
| SNPdbe | rs34712024 |
| MSV3d | rs34712024 |
| GWAS Ctlg | rs34712024 |
| Max Magnitude | 0 |
[PMID 25224256] Variants of the CNTNAP2 5' promoter as risk factors for autism spectrum disorders: a genetic and functional approach
