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: rs2297518
rs2297518
30 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 0.700 1.000 1 2013 2013
dbSNP: rs28998802
rs28998802
6 0.807 0.120 17 27797882 intron variant G/A snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs7217335
rs7217335
1 1.000 0.040 17 27771755 intron variant G/A snv 0.17 0.700 1.000 1 2019 2019
dbSNP: rs9797244
rs9797244
5 0.827 0.120 17 27770105 intron variant T/C snv 0.19 0.700 1.000 1 2016 2016