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
rs63751273 0.645 0.280 17 46010389 missense variant C/T snv 42
rs74315401 0.683 0.320 20 4699525 missense variant C/T snv 32
rs63750424 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30
rs75932628 0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs63750231 0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs63750756 0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 23
rs63750215 0.701 0.240 1 226885603 missense variant A/T snv 19
rs5848 0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17
rs63751438 0.776 0.120 17 46010388 missense variant C/T snv 16
rs367543041 0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 15
rs387906789
VCP
0.742 0.200 9 35065352 missense variant G/A;C snv 4.0E-06 14
rs63750082 0.732 0.120 14 73192712 missense variant G/C;T snv 8.0E-06 13
rs63750083 0.732 0.160 14 73219177 missense variant C/A;T snv 13
rs121909330
VCP
0.752 0.200 9 35065364 missense variant G/A;C;T snv 11
rs121909334
VCP
0.752 0.200 9 35065255 missense variant C/T snv 1.6E-05 10
rs767543900 0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 10
rs387906709 0.776 0.120 X 56565363 missense variant C/A;T snv 9
rs63750066
APP
0.763 0.160 21 25891796 missense variant C/T snv 9.5E-05 6.3E-05 9
rs63750900 0.763 0.160 14 73198067 missense variant G/A snv 4.0E-06 7.0E-06 9
rs63749824 0.776 0.120 14 73170945 missense variant C/G;T snv 4.0E-06; 1.2E-05 8
rs63749855 0.790 0.200 17 46014271 missense variant T/G snv 8
rs63750376 0.827 0.120 17 45996657 missense variant G/T snv 7
rs201258663 0.807 0.320 6 41161457 missense variant G/A snv 5.6E-05 4.9E-05 6
rs63750512 0.827 0.160 17 46024010 missense variant G/A;C snv 1.2E-05 6