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
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
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
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.010 1.000 1 2013 2013
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
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
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
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
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.010 1.000 1 2019 2019
Hypercholesterolemia, Familial
CUI: C0020445
Disease: Hypercholesterolemia, Familial
1423 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.010 1.000 1 2016 2016
Hyperlipoproteinemia Type IIa
CUI: C0745103
Disease: Hyperlipoproteinemia Type IIa
661 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.010 1.000 1 2016 2016
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
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
197 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.010 1.000 1 2017 2017
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
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.010 1.000 1 2013 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
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.010 1.000 1 2015 2015