Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1273593548 0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs752967378 0.882 0.160 3 12618580 missense variant G/A;C snv 4.0E-06 3
rs7164773 0.790 0.240 15 60775749 intron variant C/A;T snv 10
rs12947788 0.776 0.280 17 7674109 intron variant G/A snv 0.10 8
rs1799966 0.807 0.280 17 43071077 missense variant T/A;C snv 5.2E-05; 0.35 8
rs9582036 0.776 0.280 13 28311271 intron variant C/A snv 0.59 8
rs10165970 0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs10519097 0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs11943456 0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs17024869 0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs3749474 0.724 0.320 4 55434518 3 prime UTR variant C/T snv 0.33 17
rs7581886 0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs895520 0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs11549467 0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs1800440 0.653 0.440 2 38070996 missense variant T/C;G snv 0.15; 4.0E-06 29
rs3218536 0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs727503094 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 41
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72