Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 484
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 66
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1063192 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 21
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 55
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 110
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 103
rs13278062 0.807 0.200 8 23225458 non coding transcript exon variant G/A;C;T snv 8
rs7977932 0.763 0.320 12 122172836 intron variant C/G;T snv 10
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 53
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs2295080 0.695 0.320 1 11262571 upstream gene variant G/C;T snv 20
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 55
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 62
rs2250889 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 23
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 46