rs1050450, GPX1

N. diseases: 43
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.
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 0.030 1.000 3 2007 2008
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 0.030 1.000 3 2007 2008
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 0.030 1.000 3 2007 2008
Drug-Induced Liver Disease
CUI: C0860207
Disease: Drug-Induced Liver Disease
29 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 0.010 1.000 1 2010 2010
Post transplant diabetes mellitus
CUI: C1504532
Disease: Post transplant diabetes mellitus
11 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 0.010 1.000 1 2010 2010
Chronic rejection of renal transplant
CUI: C0403592
Disease: Chronic rejection of renal transplant
1 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 0.010 1.000 1 2011 2011
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 0.010 1.000 1 2012 2012
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 0.010 1.000 1 2012 2012
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 0.010 1.000 1 2012 2012
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 0.010 1.000 1 2012 2012
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 0.010 1.000 1 2012 2012
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 0.010 1.000 1 2012 2012
Peripheral Nervous System Diseases
CUI: C4721453
Disease: Peripheral Nervous System Diseases
69 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 0.010 1.000 1 2012 2012
Peripheral Neuropathy
CUI: C0031117
Disease: Peripheral Neuropathy
81 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 0.010 1.000 1 2012 2012
Prostatic Diseases
CUI: C0033575
Disease: Prostatic Diseases
4 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 0.010 1.000 1 2012 2012
Sudden sensorineural hearing loss
CUI: C4275242
Disease: Sudden sensorineural hearing loss
38 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 0.010 1.000 1 2012 2012
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 0.020 1.000 2 2012 2013
Kashin-Beck Disease
CUI: C2745963
Disease: Kashin-Beck Disease
43 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 0.010 1 2013 2013
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 0.040 1.000 4 2007 2014
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 0.040 1.000 4 2007 2014
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 0.010 1.000 1 2014 2014
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 0.010 1.000 1 2014 2014
Malignant neoplasm of urinary bladder
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
316 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 0.010 1.000 1 2014 2014
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 0.030 1.000 3 2013 2015
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 0.030 1.000 3 2013 2015