rs4363657, SLCO1B1

N. diseases: 5
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 level result
CUI: C1287365
Disease: Bilirubin level result
478 12 21215788 intron variant T/C snv 0.18 0.700 1.000 2 2009 2011
Bilirubin measurement
CUI: C0344395
Disease: Bilirubin measurement
535 12 21215788 intron variant T/C snv 0.18 0.800 1.000 2 2009 2011
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 12 21215788 intron variant T/C snv 0.18 0.020 1.000 2 2015 2019
Myalgia
CUI: C0231528
Disease: Myalgia
22 12 21215788 intron variant T/C snv 0.18 0.010 1.000 1 2015 2015
Myopathy
CUI: C0026848
Disease: Myopathy
166 12 21215788 intron variant T/C snv 0.18 0.010 1.000 1 2008 2008