Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs5742909 0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 40
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs1982073 0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs2853676 0.667 0.560 5 1288432 intron variant T/A;C snv 29
rs531564 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 27
rs3025058 0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26