rs4149056, SLCO1B1

N. diseases: 11
Source: CURATED ×
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
74 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.790 1.000 1 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
66 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