Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs3743930 0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs61816761 0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 43
rs866294686 0.683 0.480 10 102657073 stop gained C/A;T snv 43
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs2234922 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 42
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs3804099 0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs1178187217 0.683 0.480 7 21600085 missense variant G/A;T snv 4.3E-06 38
rs201943194 0.683 0.480 7 21710596 stop gained C/T snv 8.5E-05 8.4E-05 38
rs3732379 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs16969968 0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs1045485 0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs909253 0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs1034395178 0.716 0.480 22 20996071 stop gained C/A;T snv 4.0E-06; 8.0E-06 33