Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs139455627 | 0.851 | 0.240 | 21 | 44531087 | stop gained | G/A | snv | 3.2E-04 | 2.7E-04 | 14 | |
rs1554434435 | 1.000 | 7 | 44284206 | stop gained | G/A | snv | 4 | ||||
rs1559931177 | 0.827 | 0.120 | 3 | 49047207 | stop gained | G/A | snv | 34 | |||
rs387907141 | 0.752 | 0.360 | 6 | 157181137 | stop gained | C/T | snv | 24 | |||
rs387907144 | 0.716 | 0.600 | 6 | 157181056 | stop gained | C/A;T | snv | 34 | |||
rs387907329 | 0.827 | 0.200 | X | 49075573 | stop gained | G/A;T | snv | 5.5E-06 | 10 | ||
rs587782993 | 0.882 | 0.080 | 5 | 140114737 | stop gained | C/T | snv | 6 | |||
rs587782996 | 0.925 | 0.080 | 5 | 140114544 | stop gained | C/G;T | snv | 9.0E-06 | 5 | ||
rs587782997 | 0.925 | 0.080 | 5 | 140114964 | stop gained | C/G | snv | 5 | |||
rs587783405 | 0.851 | 0.160 | X | 18588021 | stop gained | C/T | snv | 9 | |||
rs878853164 | 1.000 | 0.160 | 11 | 68157849 | stop gained | C/A | snv | 4.0E-06 | 5 | ||
rs878853169 | 1.000 | 0.160 | 13 | 35550528 | stop gained | C/T | snv | 4 | |||
rs1057518961 | 0.925 | 0.040 | 14 | 102012450 | missense variant | C/T | snv | 5 | |||
rs1057519440 | 1.000 | 0.040 | X | 51744647 | missense variant | G/A | snv | 3 | |||
rs1085307993 | 0.716 | 0.440 | 5 | 161331056 | missense variant | C/T | snv | 53 | |||
rs1131692231 | 0.827 | 0.280 | 5 | 157294834 | missense variant | C/T | snv | 13 | |||
rs1131692272 | 0.851 | 0.240 | 2 | 100006808 | missense variant | C/T | snv | 9 | |||
rs121908216 | 0.882 | 0.200 | 19 | 13235702 | missense variant | C/T | snv | 7 | |||
rs121917915 | 1.000 | 0.040 | 2 | 165994176 | missense variant | C/A | snv | 3 | |||
rs1287121256 | 0.882 | 0.040 | 5 | 150256777 | missense variant | C/G;T | snv | 7.0E-06 | 9 | ||
rs145465528 | 0.882 | 0.240 | 6 | 129143976 | missense variant | C/T | snv | 6.0E-05 | 9.1E-05 | 7 | |
rs1553798675 | 0.925 | 0.080 | 3 | 192335441 | missense variant | C/T | snv | 4 | |||
rs1554386687 | 0.882 | 0.040 | 7 | 44242328 | missense variant | C/T | snv | 12 | |||
rs1555889127 | 1.000 | 0.040 | 20 | 49374625 | missense variant | C/T | snv | 6 | |||
rs267606670 | 0.790 | 0.320 | 19 | 41968837 | missense variant | C/A;T | snv | 19 |