Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs63751273 0.645 0.280 17 46010389 missense variant C/T snv 42
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
rs646776 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs63750756 0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 23
rs5848 0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17
rs143624519 0.724 0.240 17 45991484 missense variant G/A;T snv 1.5E-03; 1.2E-05 17
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 16
rs17125721 0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14
rs80356726 0.763 0.120 1 11022352 splice acceptor variant G/A snv 4.0E-06 12
rs3173615 0.807 0.200 7 12229791 missense variant C/A;G snv 0.49 12
rs76980269 0.763 0.280 12 117330794 synonymous variant G/A snv 2.8E-05 4.2E-05 10
rs121909335
VCP
0.776 0.200 9 35065351 missense variant C/T snv 8.0E-06 9
rs4795541 0.807 0.200 17 30237299 upstream gene variant A/G snv 7
rs63751294
GRN
0.827 0.120 17 44352404 stop gained C/T snv 8.0E-06 6
rs750444386 0.807 0.360 12 117268082 synonymous variant C/A;T snv 4.0E-06; 5.6E-05 6
rs63750355 0.827 0.160 3 87253472 stop gained C/T snv 5
rs63750349 0.851 0.200 17 45996638 missense variant C/G;T snv 4.0E-06 5
rs267607102 0.851 0.120 1 11022196 missense variant A/G snv 5
rs80356717 0.851 0.120 1 11018836 missense variant A/G snv 5