HMOX1, heme oxygenase 1, 3162

N. diseases: 666; N. variants: 9
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: rs2071746
rs2071746
0.708 0.320 22 35380679 intron variant A/T snv 0.49
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.010 1.000 1 2008 2008
dbSNP: rs2071746
rs2071746
0.708 0.320 22 35380679 intron variant A/T snv 0.49
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs2071747
rs2071747
0.851 0.120 22 35381192 missense variant G/C snv 4.3E-02 4.1E-02
Necrotizing enterocolitis in fetus OR newborn
Digestive System Diseases 0.010 < 0.001 1 2016 2016
dbSNP: rs2071747
rs2071747
0.851 0.120 22 35381192 missense variant G/C snv 4.3E-02 4.1E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs2071747
rs2071747
0.851 0.120 22 35381192 missense variant G/C snv 4.3E-02 4.1E-02
CUI: C0270736
Disease: Essential Tremor
Essential Tremor
Nervous System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs2071747
rs2071747
0.851 0.120 22 35381192 missense variant G/C snv 4.3E-02 4.1E-02
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
Eye Diseases 0.010 1.000 1 2012 2012
dbSNP: rs2071749
rs2071749
0.925 0.120 22 35387420 intron variant A/G snv 0.64
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2016 2016
dbSNP: rs2071749
rs2071749
0.925 0.120 22 35387420 intron variant A/G snv 0.64
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs9607267
rs9607267
1.000 0.040 22 35385214 intron variant T/C snv 0.27
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
Cardiovascular Diseases 0.010 1.000 1 2009 2009