rs10748842, NRG3

N. diseases: 8
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 0.807 0.120 10 81889983 intron variant T/C snv 0.13 0.040 1.000 4 2010 2020
Chronic schizophrenia
CUI: C0221765
Disease: Chronic schizophrenia
7 0.807 0.120 10 81889983 intron variant T/C snv 0.13 0.010 1.000 1 2020 2020
Cognition Disorders
CUI: C0009241
Disease: Cognition Disorders
47 0.807 0.120 10 81889983 intron variant T/C snv 0.13 0.010 1.000 1 2020 2020
Hirschsprung Disease
CUI: C0019569
Disease: Hirschsprung Disease
162 0.807 0.120 10 81889983 intron variant T/C snv 0.13 0.010 1.000 1 2017 2017
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 0.807 0.120 10 81889983 intron variant T/C snv 0.13 0.010 1.000 1 2020 2020
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
1451 0.807 0.120 10 81889983 intron variant T/C snv 0.13 0.010 1.000 1 2017 2017
Mood Disorders
CUI: C0525045
Disease: Mood Disorders
308 0.807 0.120 10 81889983 intron variant T/C snv 0.13 0.010 1.000 1 2017 2017
Unipolar Depression
CUI: C0041696
Disease: Unipolar Depression
225 0.807 0.120 10 81889983 intron variant T/C snv 0.13 0.010 1.000 1 2017 2017