Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1481950 1.000 0.080 8 53777725 intron variant C/A;G snv 2
rs149215094 1.000 0.080 20 58444203 missense variant G/A snv 5.6E-05 5.6E-05 2
rs752933837 1.000 0.080 19 53906776 missense variant C/A snv 4.0E-06 1.4E-05 2
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
rs17125721 0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14
rs104893875 0.742 0.120 4 89828170 missense variant C/T snv 4.0E-06 13
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
rs121912442 0.807 0.120 21 31659783 missense variant C/T snv 3.6E-05 7
rs35801418 0.827 0.120 12 40321114 missense variant A/G snv 7
rs63750376 0.827 0.120 17 45996657 missense variant G/T snv 7
rs121917767 0.827 0.120 4 41260751 missense variant C/A;G;T snv 4.0E-05; 4.0E-06; 2.0E-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
rs1178466848 0.925 0.120 20 4699785 missense variant G/A snv 2.8E-05 4
rs387907043 0.925 0.120 20 63930873 missense variant T/A;G snv 4.0E-06 3
rs407135 0.925 0.120 12 51017570 intron variant G/T snv 0.74 3
rs63751177
GRN
1.000 0.120 17 44351438 stop gained G/A snv 2
rs104893878 0.732 0.160 4 89835580 missense variant C/G snv 21
rs121912443 0.732 0.160 21 31663857 missense variant A/G snv 15
rs5030732 0.790 0.160 4 41257616 missense variant C/A snv 0.24 0.16 10
rs121909715
GSN
0.790 0.160 9 121310819 missense variant G/A;T snv 4.0E-06 8
rs1049564
PNP
0.882 0.160 14 20472447 missense variant G/A snv 0.19 0.21 6
rs587777606 0.851 0.160 11 62691300 stop gained G/A snv 4.0E-06 7.0E-06 6