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