AOC1, amine oxidase copper containing 1, 26

N. diseases: 61; N. variants: 11
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: rs17173637
rs17173637 		7 150832361 intron variant T/C snv 8.2E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 3 2013 2018
dbSNP: rs10452848
rs10452848 		7 150826456 splice region variant A/G snv 0.36
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs17173637
rs17173637 		7 150832361 intron variant T/C snv 8.2E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2013 2013
dbSNP: rs4725366
rs4725366 		1.000 0.080 7 150824966 splice region variant A/G snv 0.81
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 1 2018 2018
dbSNP: rs4725366
rs4725366 		1.000 0.080 7 150824966 splice region variant A/G snv 0.81
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 1 2018 2018
dbSNP: rs6977081
rs6977081 		1.000 0.080 7 150845427 intron variant G/T snv 0.44
CUI: C0007286
Disease: Carpal Tunnel Syndrome
Carpal Tunnel Syndrome 		Nervous System Diseases; Wounds and Injuries 0.700 1.000 1 2019 2019
dbSNP: rs6977416
rs6977416 		7 150845623 intron variant G/A snv 0.48
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs6977416
rs6977416 		7 150845623 intron variant G/A snv 0.48
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs73165526
rs73165526 		7 150834187 intron variant T/C snv 6.9E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs10156191
rs10156191 		7 150856517 missense variant C/T snv 0.26 0.33
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		Nervous System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs10240738
rs10240738 		1.000 0.080 7 150847046 intron variant C/T snv 0.59
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs1049793
rs1049793 		0.882 0.080 7 150860577 missense variant C/G;T snv 0.37 0.37
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		Nervous System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1049793
rs1049793 		0.882 0.080 7 150860577 missense variant C/G;T snv 0.37 0.37
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.010 1.000 1 2006 2006
dbSNP: rs1049793
rs1049793 		0.882 0.080 7 150860577 missense variant C/G;T snv 0.37 0.37
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.010 < 0.001 1 2009 2009
dbSNP: rs1049793
rs1049793 		0.882 0.080 7 150860577 missense variant C/G;T snv 0.37 0.37
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2008 2008
dbSNP: rs150589026
rs150589026 		1.000 0.120 7 150860616 missense variant G/A;C snv 2.0E-05; 1.2E-05
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder) 		Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs2052129
rs2052129 		7 150851884 intron variant G/T snv 0.24
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		Nervous System Diseases 0.010 1.000 1 2015 2015