rs373126732
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs373126732(A;A) |
| Make rs373126732(A;T) |
| Make rs373126732(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 11 |
| Position | 111989050 |
| Gene | DIXDC1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs373126732 |
| dbSNP (classic) | rs373126732 |
| ClinGen | rs373126732 |
| ebi | rs373126732 |
| HLI | rs373126732 |
| Exac | rs373126732 |
| Gnomad | rs373126732 |
| Varsome | rs373126732 |
| LitVar | rs373126732 |
| Map | rs373126732 |
| PheGenI | rs373126732 |
| Biobank | rs373126732 |
| 1000 genomes | rs373126732 |
| hgdp | rs373126732 |
| ensembl | rs373126732 |
| geneview | rs373126732 |
| scholar | rs373126732 |
| rs373126732 | |
| pharmgkb | rs373126732 |
| gwascentral | rs373126732 |
| openSNP | rs373126732 |
| 23andMe | rs373126732 |
| SNPshot | rs373126732 |
| SNPdbe | rs373126732 |
| MSV3d | rs373126732 |
| GWAS Ctlg | rs373126732 |
| Max Magnitude | 0 |
Rare missense variant in DIXDC1 gene possibly implicated in autism; see dx.doi.org/10.1016/j.celrep.2016.10.047
