Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2274223 0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 40
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs2178146 0.827 0.080 16 86430089 downstream gene variant T/C snv 0.31 8
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs1050450 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1042028 0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs6498486 0.776 0.200 16 13919809 upstream gene variant A/C snv 0.27 8
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs4919510 0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs1799930 0.716 0.400 8 18400593 missense variant G/A snv 0.27 0.27 17
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs12733285 0.776 0.120 1 202952912 intron variant C/T snv 0.26 12
rs3781264 0.851 0.120 10 94310618 intron variant A/G snv 0.25 5
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs16260 0.716 0.440 16 68737131 upstream gene variant C/A snv 0.24 19
rs4778889 0.683 0.480 15 81296654 intron variant T/C snv 0.24 24
rs1143623 0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs13252298 0.827 0.160 8 127082911 non coding transcript exon variant A/G snv 0.24 8
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 23
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs4998557 0.851 0.080 21 31662579 intron variant G/A snv 0.22 4