rs2306283, SLCO1B1

N. diseases: 16
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.
Hyperbilirubinemia, Neonatal
CUI: C0857007
Disease: Hyperbilirubinemia, Neonatal
15 0.742 0.320 12 21176804 missense variant A/G;T snv 0.47 0.020 1.000 2 2013 2014
Myalgia
CUI: C0231528
Disease: Myalgia
22 0.742 0.320 12 21176804 missense variant A/G;T snv 0.47 0.010 1.000 1 2012 2012
Hyperbilirubinemia
CUI: C0020433
Disease: Hyperbilirubinemia
27 0.742 0.320 12 21176804 missense variant A/G;T snv 0.47 0.020 1.000 2 2013 2016
Drug-Induced Liver Disease
CUI: C0860207
Disease: Drug-Induced Liver Disease
29 0.742 0.320 12 21176804 missense variant A/G;T snv 0.47 0.010 1 2019 2019
Cholecystolithiasis
CUI: C0947622
Disease: Cholecystolithiasis
62 0.742 0.320 12 21176804 missense variant A/G;T snv 0.47 0.010 1 2009 2009
Diarrhea
CUI: C0011991
Disease: Diarrhea
63 0.742 0.320 12 21176804 missense variant A/G;T snv 0.47 0.010 1.000 1 2016 2016
Hyperlipidemia
CUI: C0020473
Disease: Hyperlipidemia
83 0.742 0.320 12 21176804 missense variant A/G;T snv 0.47 0.030 1.000 3 2010 2018
Cholelithiasis
CUI: C0008350
Disease: Cholelithiasis
90 0.742 0.320 12 21176804 missense variant A/G;T snv 0.47 0.010 1 2009 2009
Exudative age-related macular degeneration
CUI: C0271084
Disease: Exudative age-related macular degeneration
109 0.742 0.320 12 21176804 missense variant A/G;T snv 0.47 0.010 1.000 1 2018 2018
Thrombocytopenia
CUI: C0040034
Disease: Thrombocytopenia
110 0.742 0.320 12 21176804 missense variant A/G;T snv 0.47 0.010 1.000 1 2016 2016
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.742 0.320 12 21176804 missense variant A/G;T snv 0.47 0.010 1.000 1 2014 2014
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.742 0.320 12 21176804 missense variant A/G;T snv 0.47 0.010 1.000 1 2014 2014
Malignant neoplasm of urinary bladder
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
316 0.742 0.320 12 21176804 missense variant A/G;T snv 0.47 0.010 1.000 1 2014 2014
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.742 0.320 12 21176804 missense variant A/G;T snv 0.47 0.010 1.000 1 2013 2013
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.742 0.320 12 21176804 missense variant A/G;T snv 0.47 0.010 1.000 1 2015 2015
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.742 0.320 12 21176804 missense variant A/G;T snv 0.47 0.010 1.000 1 2013 2013