Have questions? Visit https://www.reddit.com/r/SNPedia

rs2217262

From SNPedia

Orientationplus
Stabilizedplus
Make rs2217262(A;A)
Make rs2217262(A;C)
Make rs2217262(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position112156322
GeneDOCK4
is asnp
is mentioned by
dbSNPrs2217262
ebirs2217262
HLIrs2217262
Exacrs2217262
Varsomers2217262
Maprs2217262
PheGenIrs2217262
hapmaprs2217262
1000 genomesrs2217262
hgdprs2217262
ensemblrs2217262
gopubmedrs2217262
geneviewrs2217262
scholarrs2217262
googlers2217262
pharmgkbrs2217262
gwascentralrs2217262
openSNPrs2217262
23andMers2217262
23andMe allrs2217262
SNP Nexus

SNPshotrs2217262
SNPdbers2217262
MSV3drs2217262
GWAS Ctlgrs2217262
GMAF0.08127
Max Magnitude
? (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 19401682OA-icon.png] 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 24599690OA-icon.png] Family-based association study of ZNF533, DOCK4 and IMMP2L gene polymorphisms linked to autism in a northeastern Chinese Han population