rs143609523, GALNT1

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.
Child Development Disorders, Pervasive
CUI: C0008074
Disease: Child Development Disorders, Pervasive
379 18 35685266 intron variant A/G snv 5.8E-03 0.700 1.000 1 2019 2019