rs10500171, CNTNAP2

N. diseases: 1
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.
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
395 1.000 0.040 7 147183313 intron variant A/G snv 0.52 0.010 1.000 1 2010 2010