rs10494561, NMNAT2

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.
Nonorganic psychosis
CUI: C0349204
Disease: Nonorganic psychosis
98 1.000 0.040 1 183277955 intron variant C/T snv 9.4E-02 0.010 1.000 1 2017 2017
Prodromal Symptoms
CUI: C3494358
Disease: Prodromal Symptoms
4 1.000 0.040 1 183277955 intron variant C/T snv 9.4E-02 0.010 1.000 1 2017 2017
Psychotic Disorders
CUI: C0033975
Disease: Psychotic Disorders
179 1.000 0.040 1 183277955 intron variant C/T snv 9.4E-02 0.010 1.000 1 2017 2017