Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2071746
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.030 1.000 3 2010 2017
dbSNP: rs2071746
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49
CUI: C0270736
Disease: Essential Tremor
Essential Tremor 		0.020 1.000 2 2015 2017
dbSNP: rs2071746
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49
CUI: C0035258
Disease: Restless Legs Syndrome
Restless Legs Syndrome 		0.020 1.000 2 2015 2018
dbSNP: rs2071746
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2015 2015
dbSNP: rs2071746
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.010 1.000 1 2017 2017
dbSNP: rs2071746
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49
CUI: C0014867
Disease: Esophageal Varices
Esophageal Varices 		0.010 1.000 1 2018 2018
dbSNP: rs2071746
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.010 1.000 1 2014 2014
dbSNP: rs2071746
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49
CUI: C1623038
Disease: Cirrhosis
Cirrhosis 		0.010 1.000 1 2018 2018
dbSNP: rs2071746
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		0.010 1.000 1 2014 2014
dbSNP: rs2071746
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2020 2020
dbSNP: rs2071746
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell 		0.010 1.000 1 2019 2019
dbSNP: rs2071746
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		0.010 1.000 1 2018 2018
dbSNP: rs2071746
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		0.010 1.000 1 2011 2011
dbSNP: rs2071746
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2017 2017
dbSNP: rs2071746
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.010 1.000 1 2015 2015
dbSNP: rs2071746
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.010 1.000 1 2014 2014
dbSNP: rs2071746
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.010 1.000 1 2008 2008
dbSNP: rs2071746
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis 		0.010 1.000 1 2012 2012