Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11896604 0.776 0.200 2 54252062 intron variant C/A;G;T snv 8
rs121434568 0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs12521436 0.827 0.120 5 143438042 upstream gene variant G/A snv 0.21 5
rs12683422 0.742 0.240 9 27969442 intron variant C/T snv 5.7E-02 11
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs13042395 0.752 0.160 20 773867 intron variant C/T snv 5.9E-02 13
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs1408543226
XPA
0.807 0.240 9 97675558 missense variant A/G snv 7.0E-06 6
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs144779807 0.827 0.120 5 1268529 missense variant C/A;T snv 4.0E-06; 4.0E-05 7
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs148611340 0.790 0.120 19 43543621 missense variant G/A;C snv 4.0E-06; 1.2E-05 7
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs1760944 0.672 0.480 14 20454990 non coding transcript exon variant T/C;G snv 26
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs17728461 0.776 0.120 22 30202563 intron variant C/G snv 0.25 9
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48