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: rs2966449
rs2966449
2 0.925 0.160 7 5531994 intron variant C/T snv 0.41 0.010 1.000 1 2019 2019
dbSNP: rs852426
rs852426
5 0.882 0.240 7 5526722 downstream gene variant C/T snv 0.39 0.010 1.000 1 2019 2019