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: rs2292626
rs2292626
4 0.925 0.120 10 122427198 intron variant C/T snv 0.46 0.700 1.000 1 2019 2019
dbSNP: rs2421016
rs2421016
3 0.925 0.120 10 122407996 intron variant C/T snv 0.46 0.700 1.000 1 2016 2016
dbSNP: rs71486610
rs71486610
1 10 122375287 intron variant G/C snv 0.45 0.700 1.000 1 2019 2019