rs325506, LOC105379109

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.
Child Development Disorders, Pervasive
CUI: C0008074
Disease: Child Development Disorders, Pervasive
379 1.000 0.040 5 104676602 intron variant C/G;T snv 0.700 1.000 1 2019 2019
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
1451 1.000 0.040 5 104676602 intron variant C/G;T snv 0.700 1.000 1 2019 2019