Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894060 0.882 0.120 8 1780316 missense variant C/T snv 3.2E-05 7.0E-06 3
rs104894064 0.882 0.120 8 1771124 missense variant C/G;T snv 1.0E-04; 2.4E-05 3
rs144495588 0.925 0.120 8 1771553 stop gained G/C;T snv 8.0E-06; 1.2E-05 2
rs796052407 1.000 0.120 11 1759569 missense variant G/A snv 4.0E-06 4.2E-05 1
rs587776892 0.925 0.120 20 63930871 inframe deletion CTC/- delins 2
rs104894385 0.925 0.120 13 76992176 stop gained G/A;T snv 2.7E-05; 3.1E-05 2
rs28940280 0.925 0.120 13 77000580 missense variant G/A snv 8.0E-06 2
rs386833966 0.925 0.120 13 77000824 frameshift variant T/- delins 2
rs386833967 0.925 0.120 13 77000845 frameshift variant AACA/- delins 2.8E-05 2
rs386833969 0.925 0.120 13 77000918 frameshift variant AT/- delins 2
rs386833979 0.925 0.120 13 76996083 frameshift variant -/C delins 2
rs386833980 0.925 0.120 13 76996086 stop gained G/A snv 1.6E-05 3.5E-05 2
rs786204644 0.925 0.120 13 77000667 frameshift variant AT/- delins 2
rs1555273604 1.000 0.120 13 76992207 frameshift variant -/ATCCGGGCTGG delins 1
rs794729218 1.000 0.120 13 76995933 frameshift variant G/- del 1
rs63751177
GRN
1.000 0.120 17 44351438 stop gained G/A snv 2
rs750033880 0.925 0.120 7 66633302 missense variant G/A snv 1.4E-05 3
rs140948465 0.925 0.120 4 127930800 missense variant G/A;T snv 4.0E-06; 8.0E-06 2
rs587778809 0.925 0.120 4 127938781 splice donor variant A/T snv 8.0E-06 2.8E-05 2
rs137852695 0.925 0.120 1 40091398 missense variant T/A snv 7.0E-04 6.0E-04 4
rs137852700 0.851 0.120 1 40089495 stop gained G/A;C snv 2.4E-04; 1.2E-05 4
rs137852696 0.882 0.120 1 40092409 missense variant T/G snv 1.6E-05 5.6E-05 3
rs386833634 0.925 0.120 1 40092462 frameshift variant -/T delins 3.2E-05; 4.0E-06; 4.0E-06 1.4E-05 2
rs386833645 0.925 0.120 1 40097236 start lost C/T snv 1.4E-05 2
rs386833651 0.925 0.120 1 40089409 splice donor variant C/T snv 2