rs915908, CYP2E1

N. diseases: 2
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.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.925 0.160 10 133533455 intron variant G/A snv 0.12 0.010 1.000 1 2018 2018
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.925 0.160 10 133533455 intron variant G/A snv 0.12 0.010 1.000 1 2009 2009