rs1799836, MAOB

N. diseases: 7
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.
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.790 0.160 X 43768752 intron variant T/A;C snv 0.43 0.030 1.000 3 2011 2018
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.790 0.160 X 43768752 intron variant T/A;C snv 0.43 0.020 0.500 2 2011 2016
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.790 0.160 X 43768752 intron variant T/A;C snv 0.43 0.010 1.000 1 2020 2020
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
331 0.790 0.160 X 43768752 intron variant T/A;C snv 0.43 0.010 1.000 1 2019 2019
Conduct Disorder
CUI: C0149654
Disease: Conduct Disorder
18 0.790 0.160 X 43768752 intron variant T/A;C snv 0.43 0.010 1 2016 2016
Dyskinetic syndrome
CUI: C0013384
Disease: Dyskinetic syndrome
42 0.790 0.160 X 43768752 intron variant T/A;C snv 0.43 0.010 1.000 1 2018 2018
Hyperprolactinemia
CUI: C0020514
Disease: Hyperprolactinemia
10 0.790 0.160 X 43768752 intron variant T/A;C snv 0.43 0.010 1.000 1 2019 2019