Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
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
rs121912438 0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs75932628 0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs80265967 0.732 0.200 21 31667290 missense variant A/C;T snv 1.4E-03 1.2E-03 16
rs11868035 0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33 14
rs387906709 0.776 0.120 X 56565363 missense variant C/A;T snv 9
rs121909668
FUS
0.790 0.120 16 31191418 missense variant C/A;G;T snv 1.2E-05 8
rs121912433 0.827 0.120 21 31663841 missense variant G/A snv 4.0E-06 7
rs80356733 0.790 0.200 1 11022451 missense variant G/T snv 7
rs775129479 0.851 0.120 16 1791387 missense variant G/A;C;T snv 1.6E-05; 8.1E-06; 8.1E-06 6
rs781587642 0.851 0.120 2 219250557 missense variant G/A;C snv 2.0E-05 6
rs80356734 0.851 0.160 1 11022464 missense variant A/G snv 4
rs1427575965 0.925 0.120 2 70212796 missense variant G/A snv 8.0E-06 3