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: 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
dbSNP: rs2071746
rs2071746
0.708 0.320 22 35380679 intron variant A/T snv 0.49
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.030 1.000 3 2010 2017
dbSNP: rs1176147476
rs1176147476
1.000 0.040 22 35386688 missense variant G/T snv 4.0E-06
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
Respiratory Tract Diseases 0.010 1.000 1 2010 2010
dbSNP: rs2071746
rs2071746
0.708 0.320 22 35380679 intron variant A/T snv 0.49
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
Cardiovascular Diseases 0.010 1.000 1 2011 2011
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: rs11555832
rs11555832
22 35393876 3 prime UTR variant A/G;T snv
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs11555832
rs11555832
22 35393876 3 prime UTR variant A/G;T snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs17880056
rs17880056
22 35393842 3 prime UTR variant C/T snv 2.7E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs17880056
rs17880056
22 35393842 3 prime UTR variant C/T snv 2.7E-02
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs2071746
rs2071746
0.708 0.320 22 35380679 intron variant A/T snv 0.49
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis
Digestive System Diseases 0.010 1.000 1 2012 2012
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: rs8140370
rs8140370
22 35383642 intron variant T/G snv 5.6E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs8140370
rs8140370
22 35383642 intron variant T/G snv 5.6E-02
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs113683735
rs113683735
0.925 0.080 22 35386751 missense variant A/G snv
CUI: C0857007
Disease: Hyperbilirubinemia, Neonatal
Hyperbilirubinemia, Neonatal
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities 0.010 1.000 1 2013 2013
dbSNP: rs113683735
rs113683735
0.925 0.080 22 35386751 missense variant A/G snv
CUI: C0020433
Disease: Hyperbilirubinemia
Hyperbilirubinemia
Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2014 2014
dbSNP: rs2071746
rs2071746
0.708 0.320 22 35380679 intron variant A/T snv 0.49
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs2071746
rs2071746
0.708 0.320 22 35380679 intron variant A/T snv 0.49
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs2071746
rs2071746
0.708 0.320 22 35380679 intron variant A/T snv 0.49
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs2071746
rs2071746
0.708 0.320 22 35380679 intron variant A/T snv 0.49
CUI: C0035258
Disease: Restless Legs Syndrome
Restless Legs Syndrome
Nervous System Diseases; Mental Disorders 0.020 1.000 2 2015 2018
dbSNP: rs2071746
rs2071746
0.708 0.320 22 35380679 intron variant A/T snv 0.49
CUI: C0270736
Disease: Essential Tremor
Essential Tremor
Nervous System Diseases 0.020 1.000 2 2015 2017
dbSNP: rs2071746
rs2071746
0.708 0.320 22 35380679 intron variant A/T snv 0.49
Malignant neoplasm of colon and/or rectum
0.010 1.000 1 2015 2015
dbSNP: rs2071746
rs2071746
0.708 0.320 22 35380679 intron variant A/T snv 0.49
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2015 2015
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: 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