Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1567690011 | 0.882 | 0.080 | 16 | 68337496 | frameshift variant | AG/- | delins | 9 | |||
rs1567721991 | 0.882 | 0.080 | 16 | 68347257 | frameshift variant | -/GCTCTCCG | delins | 9 | |||
rs771148519 | 0.807 | 0.200 | 4 | 39225027 | stop gained | C/G | snv | 1.7E-05 | 1.4E-05 | 9 | |
rs886039813 | 0.827 | 0.160 | X | 13756600 | frameshift variant | C/- | delins | 8 | |||
rs1565311145 | 0.882 | 0.120 | 11 | 103116677 | stop gained | T/A | snv | 7 | |||
rs767846762 | 0.882 | 0.120 | 11 | 103176241 | frameshift variant | AA/- | delins | 1.0E-05 | 7 | ||
rs776587763 | 0.790 | 0.120 | 10 | 121520085 | missense variant | C/A;T | snv | 4.0E-06; 4.0E-06 | 7 | ||
rs1556165162 | 0.882 | 0.120 | X | 72572657 | frameshift variant | GG/- | delins | 7 | |||
rs1057518972 | 0.827 | 0.200 | 8 | 115418359 | missense variant | C/T | snv | 7 | |||
rs1565317399 | 0.882 | 0.120 | 11 | 103122879 | stop gained | C/T | snv | 6 | |||
rs1567499068 | 0.882 | 0.160 | 15 | 76574190 | frameshift variant | G/- | delins | 6 | |||
rs587784000 | 0.882 | 0.120 | 5 | 37044480 | missense variant | G/C;T | snv | 5 | |||
rs387906836 | 0.851 | 0.080 | 6 | 35503763 | missense variant | G/A | snv | 5 | |||
rs1057519324 | 0.925 | 0.080 | 9 | 35801153 | stop gained | C/T | snv | 7.0E-06 | 4 | ||
rs140047318 | 0.882 | 0.080 | 4 | 95152757 | missense variant | G/A;C;T | snv | 1.6E-05; 4.0E-06 | 3 | ||
rs199566527 | 0.882 | 0.080 | 17 | 56594498 | missense variant | G/A | snv | 1.7E-03 | 1.7E-03 | 3 | |
rs267607016 | 0.882 | 0.120 | 9 | 91726603 | stop gained | G/A | snv | 4.0E-06 | 1.4E-05 | 3 | |
rs77096466 | 1.000 | 0.080 | 20 | 58905474 | missense variant | C/T | snv | 1 |