rs622342, SLC22A1

N. diseases: 4
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.
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.882 0.280 6 160151834 intron variant C/A snv 0.70 0.020 1.000 2 2014 2015
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.882 0.280 6 160151834 intron variant C/A snv 0.70 0.010 1.000 1 2009 2009
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.882 0.280 6 160151834 intron variant C/A snv 0.70 0.010 1.000 1 2015 2015
Dystrophia myotonica 2
CUI: C2931689
Disease: Dystrophia myotonica 2
21 0.882 0.280 6 160151834 intron variant C/A snv 0.70 0.010 1.000 1 2013 2013