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: rs2763981
rs2763981
5 6 31872244 intron variant T/A snv 0.79 0.700 1.000 2 2019 2019
dbSNP: rs115485095
rs115485095
3 6 31888293 intron variant G/A snv 0.700 1.000 1 2018 2018
dbSNP: rs116477171
rs116477171
3 6 31918153 intron variant C/G;T snv 0.700 1.000 1 2018 2018