rs2231142, ABCG2

N. diseases: 56
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.
Uric acid measurement (procedure)
CUI: C0202239
Disease: Uric acid measurement (procedure)
1463 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.800 1.000 14 2008 2019
Gout
CUI: C0018099
Disease: Gout
2354 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.820 1.000 12 2008 2019
Arthritis, Gouty
CUI: C0003868
Disease: Arthritis, Gouty
2356 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.810 1.000 11 2008 2019
Hyperuricemia
CUI: C0740394
Disease: Hyperuricemia
76 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.800 1.000 10 2010 2019
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.040 1.000 4 2005 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.040 1.000 4 2005 2019
Diarrhea
CUI: C0011991
Disease: Diarrhea
63 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.030 1.000 3 2006 2019
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.030 1.000 3 2013 2019
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.020 1.000 2 2005 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.010 1.000 1 2019 2019
Kidney Calculi
CUI: C0022650
Disease: Kidney Calculi
71 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.010 1.000 1 2019 2019
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.010 1.000 1 2019 2019
Nephrolithiasis
CUI: C0392525
Disease: Nephrolithiasis
99 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.010 1.000 1 2019 2019
Obesity
CUI: C0028754
Disease: Obesity
1111 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.010 1.000 1 2019 2019
Primary gout
CUI: C0149896
Disease: Primary gout
5 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.010 1.000 1 2019 2019
Secondary malignant neoplasm of lymph node
CUI: C0686619
Disease: Secondary malignant neoplasm of lymph node
188 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.010 1.000 1 2019 2019
Myeloid Leukemia, Chronic
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
115 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.040 1.000 4 2013 2018
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.020 1.000 2 2016 2018
Kidney Failure, Chronic
CUI: C0022661
Disease: Kidney Failure, Chronic
425 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.700 1.000 1 2018 2018
Lesch-Nyhan Syndrome
CUI: C0023374
Disease: Lesch-Nyhan Syndrome
32 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.010 1.000 1 2018 2018
Malignant neoplasm of stomach stage IV
CUI: C0278498
Disease: Malignant neoplasm of stomach stage IV
7 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.010 1.000 1 2018 2018
Nausea
CUI: C0027497
Disease: Nausea
14 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.010 1.000 1 2018 2018
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.010 1.000 1 2018 2018
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.010 1.000 1 2018 2018
Skin toxicity
CUI: C1167791
Disease: Skin toxicity
24 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.010 1 2018 2018