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.
progesterone receptor-negative breast cancer
CUI: C4733093
Disease: progesterone receptor-negative breast cancer
11 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.010 1.000 1 2015 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
progesterone receptor-positive breast cancer
CUI: C4733094
Disease: progesterone receptor-positive breast cancer
17 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.010 1.000 1 2015 2015
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
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
Neoplasm, Residual
CUI: C0242596
Disease: Neoplasm, Residual
23 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.010 1.000 1 2017 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
Familial hypercholesterolemia - heterozygous
CUI: C0342882
Disease: Familial hypercholesterolemia - heterozygous
34 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.010 1.000 1 2006 2006
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
Renal Insufficiency
CUI: C1565489
Disease: Renal Insufficiency
42 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.010 1.000 1 2019 2019
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
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
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
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
Lymphoma, Non-Hodgkin, Familial
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
79 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.010 1.000 1 2017 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
Neutropenia
CUI: C0027947
Disease: Neutropenia
97 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.010 1.000 1 2016 2016
Exudative age-related macular degeneration
CUI: C0271084
Disease: Exudative age-related macular degeneration
109 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.010 1.000 1 2018 2018
Thrombocytopenia
CUI: C0040034
Disease: Thrombocytopenia
110 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.010 1.000 1 2016 2016
Diffuse Large B-Cell Lymphoma
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
127 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.010 1.000 1 2014 2014
Leukopenia
CUI: C0023530
Disease: Leukopenia
153 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.010 1.000 1 2016 2016
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.010 1.000 1 2019 2019
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