Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 59
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
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
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 53
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs1801157 0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 45
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 45
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 45
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 44
rs755622 0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 42
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 40
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40