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.
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
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
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
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
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
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.010 1.000 1 2018 2018
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
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
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
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