||Reduced Autism risk
||1.19x risk of Autism
||1.42x risk of Autism
23andMe blog rs4307059 — compared to two copies of a C, each copy of the more common T version increased the odds of autism by 1.19 times. 
[PMID 19404256] Common genetic variants on 5p14.1 associate with autism spectrum disorders
[PMID 20634369] Association Between a High-Risk Autism Locus on 5p14 and Social Communication Spectrum Phenotypes in the General Population
[PMID 22491950] A noncoding RNA antisense to moesin at 5p14.1 in autism
[PMID 19456320] A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.
[PMID 19812673] A genome-wide linkage and association scan reveals novel loci for autism.
[PMID 22739633] The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families
[PMID 22846907] Analysis of four genes involved in the neurodevelopment shows association of rs4307059 polymorphism in the cadherin 9/10 region with completed suicide.
[PMID 33076578] Genetic Risk of Autism Spectrum Disorder in a Pakistani Population.