Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs187115 0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs1990172 0.827 0.120 7 20164512 intron variant A/C snv 0.27 6
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 47
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 36
rs2298881 0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs2735971 0.790 0.240 11 2000419 intron variant T/C snv 7
rs3116496 0.776 0.160 2 203729789 intron variant T/C snv 0.15 0.14 11
rs3757441 0.752 0.200 7 148827660 intron variant C/T snv 0.80 12
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs7421861 0.790 0.200 2 241853198 intron variant A/G;T snv 9
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs10012 0.716 0.280 2 38075247 missense variant G/C snv 0.31 0.36 16
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1050450 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs11556218 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 26
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 62