Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11558538 0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 19
rs2071746 0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs1143633 0.752 0.280 2 112832890 intron variant C/G;T snv 11
rs1052553 0.827 0.200 17 45996523 synonymous variant A/G snv 0.14 0.15 8
rs3794087 0.851 0.120 11 35308068 intron variant G/T snv 0.20 6
rs3810651 0.925 0.080 X 152652814 missense variant A/C;T snv 4