Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
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
rs3173615 0.807 0.200 7 12229791 missense variant C/A;G snv 0.49 12
rs80356726 0.763 0.120 1 11022352 splice acceptor variant G/A snv 4.0E-06 12
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
rs2234253 0.827 0.120 6 41161367 missense variant G/A;C;T snv 1.9E-04; 1.0E-02 5
rs267607102 0.851 0.120 1 11022196 missense variant A/G snv 5
rs63750349 0.851 0.200 17 45996638 missense variant C/G;T snv 4.0E-06 5
rs63750355 0.827 0.160 3 87253472 stop gained C/T snv 5
rs80356717 0.851 0.120 1 11018836 missense variant A/G snv 5
rs63750129 0.882 0.120 17 45996612 missense variant A/C snv 4.0E-06 4
rs63750541
GRN
0.851 0.160 17 44351586 missense variant G/A;C snv 8.4E-04 4
rs63751243
GRN
0.882 0.160 17 44349190 missense variant C/A;T snv 4.0E-06 4
rs753070659
GRN
0.851 0.160 17 44350481 missense variant G/A;C snv 1.2E-05 4
rs63750092 0.882 0.120 17 46014277 missense variant A/T snv 3
rs63751180
GRN
0.882 0.120 17 44352087 stop gained C/A;G;T snv 4.0E-06; 4.0E-06 3
rs1319062081 0.925 0.120 21 31668537 stop gained G/T snv 2