rs184718561
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs184718561(C;C) |
| Make rs184718561(C;T) |
| Make rs184718561(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 11 |
| Position | 112016769 |
| Gene | DIXDC1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs184718561 |
| dbSNP (classic) | rs184718561 |
| ClinGen | rs184718561 |
| ebi | rs184718561 |
| HLI | rs184718561 |
| Exac | rs184718561 |
| Gnomad | rs184718561 |
| Varsome | rs184718561 |
| LitVar | rs184718561 |
| Map | rs184718561 |
| PheGenI | rs184718561 |
| Biobank | rs184718561 |
| 1000 genomes | rs184718561 |
| hgdp | rs184718561 |
| ensembl | rs184718561 |
| geneview | rs184718561 |
| scholar | rs184718561 |
| rs184718561 | |
| pharmgkb | rs184718561 |
| gwascentral | rs184718561 |
| openSNP | rs184718561 |
| 23andMe | rs184718561 |
| SNPshot | rs184718561 |
| SNPdbe | rs184718561 |
| MSV3d | rs184718561 |
| GWAS Ctlg | rs184718561 |
| Max Magnitude | 0 |
Rare missense variant in DIXDC1 gene possibly implicated in autism; see dx.doi.org/10.1016/j.celrep.2016.10.047
