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: rs742071
rs742071
2 0.925 0.120 1 18653380 intron variant G/T snv 0.39 0.700 1.000 1 2017 2017
dbSNP: rs9439713
rs9439713
3 0.882 0.120 1 18646282 intron variant G/A snv 0.31 0.700 1.000 1 2017 2017
dbSNP: rs9439714
rs9439714
3 0.882 0.120 1 18649995 intron variant T/C snv 0.28 0.700 1.000 1 2017 2017