Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 61
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 55
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 55
rs759412116 0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 55
rs2228000
XPC
0.585 0.560 3 14158387 missense variant G/A snv 0.24 0.21 53
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 47
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 45
rs1050450 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs1805794
NBN
0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 41
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs2274223 0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 39
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38