Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs1050450 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs4646903 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 36
rs763351020 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35
rs1061622 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33