{{Rsnum
|rsid=1922892
|Gene=CNTNAP2
|Chromosome=7
|position=147879319
|Orientation=plus
|GMAF=0.4008
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=CNTNAP2
}}Reported to be in very tight (r<sup>2</sup>>0.98) linkage with [[rs2710102]], and thus potentially associated with [[autism]].

{{PMID|18987363|OA=1
}} [[Speech]] development [[rs4431523]], [[rs17236239]] and significant associations (with P values from 0.01 to 5.0x10–5) between nonsense-word repetition and nine intronic SNPs ([[rs851715]], [[rs10246256]], [[rs2710102]], [[rs759178]], [[rs1922892]], [[rs2538991]], [[rs17236239]], [[rs2538976]], and [[rs2710117]])

{{PMID|18179893|OA=1
}} Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene.

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}