The ''C'' allele was associated with autism spectrum disorder (ASD) (P=0.033)  [R1, R2].

''C'' allele occurence was consistent in families with autism and gastrointestinal conditions. ''C'' allele from parent to child was consistently associated with both social and communication phenotypes of autism [R1, R2].

A significant increase in the ''C'' allele variant frequency was found in Autistic Disorder patients as compared to Controls (chi(2)=5.8, df=1, P=0.02) [R].




Parent Gene: MET

Importance: 2
Less common allele: G = 46%
More common allele: C = 54%
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