Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs78378222 0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs745934102 0.882 0.040 1 13607281 missense variant G/A snv 3.2E-05 1.4E-05 5
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs603965 0.732 0.440 11 69648142 splice region variant G/A snv 14
rs6010620 0.701 0.360 20 63678486 intron variant A/C;G snv 21
rs55819519 0.627 0.400 17 7673751 missense variant C/A;G;T snv 1.6E-04 1.3E-04 40
rs4977756 0.683 0.440 9 22068653 intron variant G/A snv 0.64 24
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs374052197 0.882 0.040 1 13610421 missense variant G/A;T snv 8.0E-06 5
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 37
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1800371 0.742 0.240 17 7676230 missense variant G/A;T snv 1.2E-03 15
rs1799969 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1273593548 0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19