rs55661361, NRGN

N. diseases: 3
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.
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 1.000 0.040 11 124744061 intron variant G/A snv 0.43 0.700 1.000 8 2014 2019
Child Development Disorders, Pervasive
CUI: C0008074
Disease: Child Development Disorders, Pervasive
379 1.000 0.040 11 124744061 intron variant G/A snv 0.43 0.700 1.000 2 2017 2019
Intelligence
CUI: C0021704
Disease: Intelligence
2093 1.000 0.040 11 124744061 intron variant G/A snv 0.43 0.700 1.000 1 2019 2019