Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10230087
rs10230087
Entrez Id: 93986
Gene Symbol: FOXP2
FOXP2
CUI: C1510586
Disease:
Autism Spectrum Disorders
0.010 GeneticVariation BEFREE In interaction analysis, the FOXP2-TCGC (rs12531289-rs1350135-rs10230087-rs2061183) diplotype and MAOA-TCG (rs6323-rs1801291-rs3027407) haplotype were significantly associated with autism spectrum disorder in males. 24356376 2014