rs1620977, NEGR1

N. diseases: 3
Source: GWASCAT ×
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 1 72263459 intron variant A/G;T snv 0.700 1.000 1 2019 2019
Intelligence
CUI: C0021704
Disease: Intelligence
2089 1.000 0.040 1 72263459 intron variant A/G;T snv 0.700 1.000 1 2018 2018
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
963 1.000 0.040 1 72263459 intron variant A/G;T snv 0.700 1.000 1 2019 2019