Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6877842 0.807 0.320 5 31532531 intron variant G/C snv 0.16 7
rs4789223 0.851 0.120 17 75645819 intron variant G/A snv 0.46 4
rs1816158 0.925 0.200 11 122155752 intron variant C/A;T snv 3
rs3213282 0.882 0.160 19 43568728 intron variant G/C snv 0.57 3
rs3810378 1.000 0.120 19 43577449 intron variant G/C snv 0.29 3
rs4725443 0.925 0.120 7 152170176 intron variant T/C snv 9.3E-02 2
rs50871 0.925 0.120 19 45359257 intron variant C/A snv 0.64 2
rs6943984 0.925 0.120 7 152201919 intron variant G/A snv 0.11 2
rs1799778 1.000 0.120 19 43554989 intron variant G/T snv 0.31 1
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs34301344 0.689 0.400 13 49630893 stop gained G/A snv 9.7E-03 7.9E-03 22
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs759412116 0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 55