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: rs2000999
rs2000999
7 1.000 0.080 16 72074194 intron variant G/A snv 0.16 0.800 1.000 6 2010 2018
dbSNP: rs217184
rs217184
2 16 72072066 intron variant T/C snv 0.19 0.700 1.000 1 2019 2019