rs10230087, FOXP2

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
331 1.000 0.040 7 114614352 intron variant G/A snv 0.73 0.010 1.000 1 2014 2014
Pervasive Development Disorder
CUI: C0524528
Disease: Pervasive Development Disorder
49 1.000 0.040 7 114614352 intron variant G/A snv 0.73 0.010 1.000 1 2014 2014