Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4537545 0.790 0.160 1 154446403 intron variant C/T snv 0.48 11
rs7744 0.827 0.160 3 38142530 3 prime UTR variant A/G snv 0.13 5
rs4251961 0.763 0.200 2 113116890 intron variant T/C snv 0.29 10
rs428253 0.851 0.200 19 4229916 intron variant G/C snv 0.33 4
rs17293632 0.763 0.240 15 67150258 intron variant C/T snv 0.17 12
rs4740 0.827 0.240 19 4236999 missense variant G/A snv 0.34 0.39 8
rs9471535 0.851 0.240 6 41287752 upstream gene variant T/C snv 0.12 5
rs1239681664 0.716 0.320 9 104818690 synonymous variant A/G snv 7.0E-06 15
rs3748067 0.672 0.320 6 52190541 3 prime UTR variant C/T snv 6.2E-02 21
rs1131498 0.732 0.360 1 169707345 missense variant A/G snv 0.21 0.22 13
rs1801198 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 26
rs10754558 0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs2043211 0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs696 0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45 22
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs763351020 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs3732379 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57