MAOB, monoamine oxidase B, 4129

N. diseases: 152; N. variants: 8
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1799836
rs1799836
0.790 0.160 X 43768752 intron variant T/A;C snv 0.43
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.030 1.000 3 2011 2018
dbSNP: rs1799836
rs1799836
0.790 0.160 X 43768752 intron variant T/A;C snv 0.43
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.020 0.500 2 2011 2016
dbSNP: rs1799836
rs1799836
0.790 0.160 X 43768752 intron variant T/A;C snv 0.43
CUI: C0020514
Disease: Hyperprolactinemia
Hyperprolactinemia
Nervous System Diseases; Endocrine System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs1799836
rs1799836
0.790 0.160 X 43768752 intron variant T/A;C snv 0.43
CUI: C0013384
Disease: Dyskinetic syndrome
Dyskinetic syndrome
Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1799836
rs1799836
0.790 0.160 X 43768752 intron variant T/A;C snv 0.43
CUI: C0149654
Disease: Conduct Disorder
Conduct Disorder
Mental Disorders 0.010 < 0.001 1 2016 2016
dbSNP: rs1799836
rs1799836
0.790 0.160 X 43768752 intron variant T/A;C snv 0.43
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs1799836
rs1799836
0.790 0.160 X 43768752 intron variant T/A;C snv 0.43
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.010 1.000 1 2020 2020
dbSNP: rs2283727
rs2283727
1.000 0.040 X 43773697 intron variant G/A;T snv
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
Mental Disorders 0.010 1.000 1 2016 2016
dbSNP: rs2283728
rs2283728
1.000 0.040 X 43773881 intron variant G/A;C snv
Attention deficit hyperactivity disorder
Mental Disorders 0.010 1.000 1 2016 2016
dbSNP: rs3027440
rs3027440
1.000 0.040 X 43767234 3 prime UTR variant A/G snv 2.4E-02
Attention deficit hyperactivity disorder
Mental Disorders 0.010 1.000 1 2016 2016
dbSNP: rs3027452
rs3027452
1.000 0.040 X 43798542 intron variant G/A snv 0.13
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease
Endocrine System Diseases 0.010 1.000 1 2020 2020
dbSNP: rs56220155
rs56220155
1.000 0.040 X 43773915 intron variant T/C snv 0.30
Attention deficit hyperactivity disorder
Mental Disorders 0.010 1.000 1 2016 2016
dbSNP: rs5905512
rs5905512
1.000 0.040 X 43867148 intron variant A/G snv
CUI: C0033975
Disease: Psychotic Disorders
Psychotic Disorders
Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs5905512
rs5905512
1.000 0.040 X 43867148 intron variant A/G snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs6324
rs6324
X 43767568 synonymous variant G/A snv 5.0E-02 2.5E-02
CUI: C0004941
Disease: Behavioral Symptoms
Behavioral Symptoms
Behavior and Behavior Mechanisms 0.010 1.000 1 2016 2016