Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3176352 0.807 0.120 6 36684562 intron variant C/A;G;T snv 8.0E-06; 0.37; 2.0E-05 7
rs246079
UNG
0.790 0.120 12 109109255 intron variant A/G;T snv 9
rs11674595 0.763 0.200 2 101994530 intron variant T/C snv 0.22 13
rs786202962 0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 21
rs587782329 0.677 0.280 17 7674217 missense variant C/A;G;T snv 23
rs3787016 0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs568408 0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16 29
rs2234767 0.649 0.280 10 88989499 intron variant G/A;T snv 0.15 30
rs763110 0.653 0.560 1 172658358 upstream gene variant C/T snv 0.49 30
rs1800682 0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs4646903 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 36
rs752742313 0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105