Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs2104286 0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs5029939 0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
rs11889341 0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs3131379 0.752 0.440 6 31753256 intron variant G/A snv 6.4E-02 7.9E-02 10
rs1518111 0.790 0.360 1 206771300 intron variant T/C snv 0.71 9
rs1678542 0.790 0.320 12 57574932 intron variant C/G snv 0.42 9
rs12583006 0.807 0.320 13 108285104 intron variant T/A snv 0.21 8
rs1341239 0.776 0.360 6 22303975 intron variant A/C snv 0.65 8
rs292001 0.807 0.320 1 22638465 intron variant G/A snv 0.54 6
rs1518110 0.851 0.160 1 206771516 intron variant A/C;T snv 5
rs13023380 0.851 0.160 2 162297853 intron variant G/A snv 0.35 4
rs1876453
CR2
0.851 0.160 1 207454573 intron variant G/A snv 8.4E-02 4
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 9
rs2205960 0.763 0.400 1 173222336 intergenic variant G/A;T snv 9
rs10489265 0.827 0.200 1 173266926 regulatory region variant A/C snv 0.21 5
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs121908117 0.708 0.440 3 48466707 missense variant G/A snv 17
rs1050501 0.732 0.440 1 161674008 missense variant T/C snv 0.16 0.19 15
rs1143679 0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs2397084 0.716 0.480 6 52237046 missense variant T/C snv 6.7E-02 6.1E-02 14