Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 8
rs822396 0.732 0.400 3 186849088 intron variant G/A snv 0.81 16
rs2794521
CRP
0.742 0.480 1 159715306 upstream gene variant C/T snv 0.78 15
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs3774261 0.776 0.320 3 186853770 splice region variant A/G snv 0.55 10
rs7044343 0.752 0.520 9 6254208 intron variant C/T snv 0.51 13
rs20455 0.763 0.160 6 39357302 missense variant A/G snv 0.41 0.49 12
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1333048 0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs9937053
FTO
0.882 0.160 16 53765595 intron variant G/A snv 0.42 6
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs2230806 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs12495941 0.851 0.280 3 186850391 intron variant G/T snv 0.35 5
rs4986938 0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33 35
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21