Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11196067 0.752 0.160 10 112709306 intron variant A/T snv 0.32 10
rs16906252 0.732 0.200 10 129467281 synonymous variant C/T snv 5.5E-02 5.1E-02 17
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs562015640 0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 15
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs1801198 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 26
rs121918464 0.708 0.440 12 112450406 missense variant G/A;C snv 19
rs3856806 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 40
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 83
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 46
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 47
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 135
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 57
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 103
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 47
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 97
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242