Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104893877 0.614 0.360 4 89828149 missense variant C/T snv 59
rs121912438 0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs74315401 0.683 0.320 20 4699525 missense variant C/T snv 32
rs75932628 0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs1799990 0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 23
rs63750756 0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 23
rs143624519 0.724 0.240 17 45991484 missense variant G/A;T snv 1.5E-03; 1.2E-05 17
rs5848 0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 16
rs63751438 0.776 0.120 17 46010388 missense variant C/T snv 16
rs3173615 0.807 0.200 7 12229791 missense variant C/A;G snv 0.49 12
rs121909329
VCP
0.763 0.200 9 35065363 missense variant C/A;G;T snv 11
rs34015634 0.851 0.120 12 40340380 missense variant T/C snv 3.2E-05 1.4E-05 8
rs63750570 0.827 0.120 17 46018629 missense variant G/A snv 8
rs63750376 0.827 0.120 17 45996657 missense variant G/T snv 7
rs63750869 0.827 0.160 17 46018707 missense variant G/A snv 2.4E-05 5.6E-05 6
rs63751068 0.827 0.120 14 73186920 missense variant G/C;T snv 6
rs63751294
GRN
0.827 0.120 17 44352404 stop gained C/T snv 8.0E-06 6
rs72824905 0.827 0.200 16 81908423 missense variant C/G;T snv 5.2E-03 6