rs4149056, SLCO1B1

N. diseases: 45
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.
Bilirubin measurement
CUI: C0344395
Disease: Bilirubin measurement
535 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.800 1.000 1 2009 2009
Myopathy
CUI: C0026848
Disease: Myopathy
166 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.790 1.000 9 2008 2019
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.700 1.000 2 2018 2018
Bilirubin level result
CUI: C1287365
Disease: Bilirubin level result
478 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.700 1.000 1 2009 2009
Estradiol level result
CUI: C1443016
Disease: Estradiol level result
75 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.700 1.000 1 2012 2012
Estradiol measurement
CUI: C0337434
Disease: Estradiol measurement
75 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.700 1.000 1 2012 2012
Finding of Mean Corpuscular Hemoglobin
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
1206 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.700 1.000 1 2019 2019
Sex hormone binding globulin measurement
CUI: C0202218
Disease: Sex hormone binding globulin measurement
21 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.700 1.000 1 2012 2012
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.700 1.000 1 2012 2012
Thyroxine measurement
CUI: C0202231
Disease: Thyroxine measurement
42 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.700 1.000 1 2018 2018
Uric acid measurement (procedure)
CUI: C0202239
Disease: Uric acid measurement (procedure)
1463 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.700 1.000 1 2019 2019
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.040 1.000 4 2015 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.040 1.000 4 2015 2019
Diarrhea
CUI: C0011991
Disease: Diarrhea
63 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.030 1.000 3 2016 2017
Hyperlipidemia
CUI: C0020473
Disease: Hyperlipidemia
83 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.030 1.000 3 2010 2018
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
261 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.020 1.000 2 2014 2019
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.020 1.000 2 2007 2017
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.020 1.000 2 2007 2017
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.020 1.000 2 2007 2017
Human immunodeficiency virus (HIV) II infection category B1
CUI: C3854222
Disease: Human immunodeficiency virus (HIV) II infection category B1
56 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.020 1.000 2 2010 2017
Hyperbilirubinemia
CUI: C0020433
Disease: Hyperbilirubinemia
27 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.020 1.000 2 2013 2015
Hyperbilirubinemia, Neonatal
CUI: C0857007
Disease: Hyperbilirubinemia, Neonatal
15 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.020 1.000 2 2014 2019
Myalgia
CUI: C0231528
Disease: Myalgia
22 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.020 1.000 2 2012 2013
Adult Non-Hodgkin Lymphoma
CUI: C0220605
Disease: Adult Non-Hodgkin Lymphoma
39 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.010 1.000 1 2017 2017
Childhood Non-Hodgkin Lymphoma
CUI: C0220612
Disease: Childhood Non-Hodgkin Lymphoma
39 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.010 1.000 1 2017 2017