rs2217262
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2217262(A;A) |
| Make rs2217262(A;C) |
| Make rs2217262(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 112156322 |
| Gene | DOCK4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2217262 |
| dbSNP (classic) | rs2217262 |
| ClinGen | rs2217262 |
| ebi | rs2217262 |
| HLI | rs2217262 |
| Exac | rs2217262 |
| Gnomad | rs2217262 |
| Varsome | rs2217262 |
| LitVar | rs2217262 |
| Map | rs2217262 |
| PheGenI | rs2217262 |
| Biobank | rs2217262 |
| 1000 genomes | rs2217262 |
| hgdp | rs2217262 |
| ensembl | rs2217262 |
| geneview | rs2217262 |
| scholar | rs2217262 |
| rs2217262 | |
| pharmgkb | rs2217262 |
| gwascentral | rs2217262 |
| openSNP | rs2217262 |
| 23andMe | rs2217262 |
| SNPshot | rs2217262 |
| SNPdbe | rs2217262 |
| MSV3d | rs2217262 |
| GWAS Ctlg | rs2217262 |
| GMAF | 0.08127 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
23andMe blog Wach copy of the A version of rs2217262 in the DOCK4 gene increased the odds of autism by 2.28 times. Note that almost 90% of people with European ancestry have two copies of the A version of this SNP, meaning that these results really mean that the rare C version of the SNP is protective against autism.
[PMID 19401682
] High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility
[PMID 24599690] Family-based association study of ZNF533, DOCK4 and IMMP2L gene polymorphisms linked to autism in a northeastern Chinese Han population
