Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs198388 0.851 0.160 1 11857283 downstream gene variant C/G;T snv 4
rs2128739 0.925 0.080 11 103802549 intron variant A/C snv 0.68 2
rs2243115 0.776 0.320 3 159988493 intron variant T/G snv 0.10 12
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs3025058 0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
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
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs633185 0.925 0.080 11 100722807 intron variant G/A;C snv 10
rs8046697 0.925 0.080 16 75408246 intron variant T/C snv 0.51 2
rs8108474 0.925 0.080 19 45798221 intron variant C/A;T snv 2
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3811381
CR1
0.763 0.240 1 207616743 missense variant C/A;G snv 8.0E-06; 0.24 11
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53