rs6584400, NRG3

N. diseases: 6
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 0.851 0.120 10 81896770 intron variant G/A snv 0.22 0.030 1.000 3 2010 2013
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
839 0.851 0.120 10 81896770 intron variant G/A snv 0.22 0.010 1.000 1 2013 2013
Cognition Disorders
CUI: C0009241
Disease: Cognition Disorders
47 0.851 0.120 10 81896770 intron variant G/A snv 0.22 0.010 1.000 1 2013 2013
Hirschsprung Disease
CUI: C0019569
Disease: Hirschsprung Disease
162 0.851 0.120 10 81896770 intron variant G/A snv 0.22 0.010 1.000 1 2017 2017
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 0.851 0.120 10 81896770 intron variant G/A snv 0.22 0.010 1.000 1 2013 2013
Psychotic symptom
CUI: C0871189
Disease: Psychotic symptom
21 0.851 0.120 10 81896770 intron variant G/A snv 0.22 0.010 1.000 1 2013 2013