Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1536826
rs1536826
CYP2E1
1 1.000 0.120 10 133543735 intron variant A/C snv 0.62 0.010 1.000 1 2009 2009