Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912438 0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs1475170339 0.732 0.240 16 1792325 missense variant T/C;G snv 18
rs121912443 0.732 0.160 21 31663857 missense variant A/G snv 15
rs74315431 0.732 0.080 20 58418318 missense variant C/T snv 4.0E-06 15
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
rs121912431 0.742 0.160 21 31663829 missense variant G/A;C snv 11
rs137852972 0.752 0.240 11 62702499 missense variant T/C snv 1.6E-05 10
rs267606673 0.776 0.240 X 78029314 missense variant C/T snv 9
rs121912436 0.827 0.080 21 31667274 missense variant G/A;C snv 7
rs762060740 0.827 0.080 17 44915083 missense variant G/C snv 4.0E-06 6
rs121909342 0.827 0.200 2 74378104 missense variant C/G;T snv 5
rs121912437 0.851 0.080 21 31667298 missense variant G/A;C;T snv 5
rs200161705 0.882 0.160 4 169585374 missense variant C/A;T snv 6.0E-05; 2.3E-03 5
rs121912439 0.851 0.080 21 31667320 missense variant A/G snv 4
rs1239669755 0.851 0.080 3 197960384 missense variant C/T snv 4
rs587777574 0.882 0.040 22 23767459 missense variant G/A snv 4
rs63750541
GRN
0.851 0.160 17 44351586 missense variant G/A;C snv 8.4E-04 4
rs747481280 0.851 0.120 10 13132068 missense variant T/G snv 8.0E-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
rs764735825 0.882 0.120 9 83707518 missense variant C/A snv 2.1E-05 3
rs772918193 0.882 0.080 17 32208230 missense variant C/G;T snv 3
rs80356719 0.882 0.080 1 11022268 missense variant G/A;C snv 1.6E-05 3
rs879253928 0.882 0.080 11 62705433 missense variant A/G snv 3