rs113764414, EGR2

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 10 62889636 intron variant A/G snv 3.6E-04 0.700 1.000 1 2019 2019