Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4759314 0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs4635002 0.925 0.080 10 127064415 intron variant A/C snv 0.92 3
rs1760893 0.807 0.080 14 20412501 intron variant C/A snv 0.89 6
rs629367 0.776 0.200 11 122146306 intron variant C/A snv 0.88 11
rs7853122 0.925 0.080 9 131705224 intron variant C/T snv 0.87 3
rs40239
MET
0.851 0.120 7 116677823 intron variant G/A snv 0.87 4
rs1279599 0.925 0.080 6 110879025 intron variant G/A snv 0.87 2
rs2494752 0.790 0.120 14 104797271 upstream gene variant A/G snv 0.85 10
rs1047972 0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19
rs1051690 0.851 0.080 19 7116952 3 prime UTR variant T/C snv 0.83 4
rs1679709 0.925 0.080 6 28260564 missense variant A/G snv 0.87 0.83 2
rs5030625 0.882 0.160 16 68736944 upstream gene variant A/- del 0.80 3
rs1864169 0.851 0.200 14 81203689 intron variant G/T snv 0.78 5
rs526934 0.925 0.080 11 59866020 intron variant G/A snv 0.77 2
rs751402 0.724 0.360 13 102845848 5 prime UTR variant A/G snv 0.76 15
rs1520220 0.807 0.280 12 102402744 intron variant G/C;T snv 0.76 9
rs8193036 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
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
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs10022537 0.925 0.080 4 16075214 intron variant A/T snv 0.70 2
rs461404 0.925 0.080 5 40799438 upstream gene variant G/A snv 0.70 3
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 53
rs10421916 0.925 0.080 19 17818178 intron variant A/G snv 0.69 2
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 70