Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121918813 1.000 0.080 2 165991892 missense variant C/G;T snv 1
rs575368466 1.000 0.080 2 165994211 missense variant C/T snv 4.0E-06 1
rs121917910 1.000 0.080 2 166009797 missense variant T/A snv 6.1E-04 6.9E-04 1
rs121917930 1.000 0.080 2 166013839 missense variant A/G snv 1
rs121917976 0.882 0.080 2 165992341 missense variant C/G;T snv 1
rs121918626 0.925 0.080 2 166012179 missense variant T/G snv 1
rs121918627 1.000 0.080 2 166002473 missense variant A/G snv 1
rs121918783 0.925 0.080 2 165991720 missense variant A/G snv 1
rs1131691773 1.000 0.080 2 165991675 missense variant A/G snv 1
rs121917932 1.000 0.080 2 165992215 missense variant A/G snv 1
rs121917955 0.925 0.080 2 165992307 missense variant G/C;T snv 1
rs121917906 1.000 0.080 2 166073542 missense variant C/G snv 8.8E-05 5.6E-05 1
rs121917953 0.851 0.080 2 166054677 missense variant T/A snv 1
rs121917984 0.790 0.080 2 166052869 missense variant G/A;C snv 1
rs121918631 0.882 0.080 2 166056450 stop gained A/G;T snv 1
rs121918781 1.000 0.080 2 166047635 missense variant A/G snv 1
rs121918782 0.882 0.080 2 166041277 missense variant T/A;C snv 1.6E-05 1
rs398123588 0.827 0.080 2 166039436 missense variant C/T snv 8.0E-06 1
rs121917954 0.925 0.080 2 166002699 missense variant C/A;G snv 1
rs121918811 0.882 0.080 2 165992306 missense variant G/A snv 7.0E-06 1
rs121918812 1.000 0.080 2 165992050 missense variant T/C snv 1
rs121918814 1.000 0.080 2 165991706 missense variant C/A snv 1
rs140731963 1.000 0.080 2 166012239 missense variant G/A snv 4.1E-04 2.6E-04 1
rs121918815 1.000 0.080 2 165991679 missense variant C/A snv 1
rs121917931 1.000 0.080 2 166073402 missense variant A/G snv 1