rs150447075
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs150447075(G;G) |
| Make rs150447075(G;T) |
| Make rs150447075(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 146115955 |
| Gene | CNTNAP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs150447075 |
| dbSNP (classic) | rs150447075 |
| ClinGen | rs150447075 |
| ebi | rs150447075 |
| HLI | rs150447075 |
| Exac | rs150447075 |
| Gnomad | rs150447075 |
| Varsome | rs150447075 |
| LitVar | rs150447075 |
| Map | rs150447075 |
| PheGenI | rs150447075 |
| Biobank | rs150447075 |
| 1000 genomes | rs150447075 |
| hgdp | rs150447075 |
| ensembl | rs150447075 |
| geneview | rs150447075 |
| scholar | rs150447075 |
| rs150447075 | |
| pharmgkb | rs150447075 |
| gwascentral | rs150447075 |
| openSNP | rs150447075 |
| 23andMe | rs150447075 |
| SNPshot | rs150447075 |
| SNPdbe | rs150447075 |
| MSV3d | rs150447075 |
| GWAS Ctlg | rs150447075 |
| Max Magnitude | 0 |
[PMID 25224256] Variants of the CNTNAP2 5' promoter as risk factors for autism spectrum disorders: a genetic and functional approach
