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: rs762551
rs762551
CYP1A2
23 0.701 0.400 15 74749576 intron variant C/A snv 0.67 0.020 1.000 2 2017 2019
dbSNP: rs2470890
rs2470890
CYP1A2
12 0.742 0.320 15 74755085 synonymous variant T/C snv 0.57 0.010 1.000 1 2014 2014