rs2071746, HMOX1

N. diseases: 18
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 0.708 0.320 22 35380679 intron variant A/T snv 0.49 0.030 1.000 3 2010 2017
Essential Tremor
CUI: C0270736
Disease: Essential Tremor
79 0.708 0.320 22 35380679 intron variant A/T snv 0.49 0.020 1.000 2 2015 2017
Restless Legs Syndrome
CUI: C0035258
Disease: Restless Legs Syndrome
72 0.708 0.320 22 35380679 intron variant A/T snv 0.49 0.020 1.000 2 2015 2018
Acute pancreatitis
CUI: C0001339
Disease: Acute pancreatitis
51 0.708 0.320 22 35380679 intron variant A/T snv 0.49 0.010 1.000 1 2012 2012
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.708 0.320 22 35380679 intron variant A/T snv 0.49 0.010 1.000 1 2008 2008
Anemia, Sickle Cell
CUI: C0002895
Disease: Anemia, Sickle Cell
138 0.708 0.320 22 35380679 intron variant A/T snv 0.49 0.010 1.000 1 2019 2019
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.708 0.320 22 35380679 intron variant A/T snv 0.49 0.010 1.000 1 2014 2014
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.708 0.320 22 35380679 intron variant A/T snv 0.49 0.010 1.000 1 2014 2014
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.708 0.320 22 35380679 intron variant A/T snv 0.49 0.010 1.000 1 2014 2014
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
110 0.708 0.320 22 35380679 intron variant A/T snv 0.49 0.010 1.000 1 2018 2018
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.708 0.320 22 35380679 intron variant A/T snv 0.49 0.010 1.000 1 2015 2015
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.708 0.320 22 35380679 intron variant A/T snv 0.49 0.010 1.000 1 2017 2017
Esophageal Varices
CUI: C0014867
Disease: Esophageal Varices
5 0.708 0.320 22 35380679 intron variant A/T snv 0.49 0.010 1.000 1 2018 2018
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.708 0.320 22 35380679 intron variant A/T snv 0.49 0.010 1.000 1 2011 2011
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.708 0.320 22 35380679 intron variant A/T snv 0.49 0.010 1.000 1 2020 2020
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.708 0.320 22 35380679 intron variant A/T snv 0.49 0.010 1.000 1 2017 2017
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.708 0.320 22 35380679 intron variant A/T snv 0.49 0.010 1.000 1 2018 2018
Malignant neoplasm of colon and/or rectum
502 0.708 0.320 22 35380679 intron variant A/T snv 0.49 0.010 1.000 1 2015 2015