Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs76763715 | 0.658 | 0.520 | 1 | 155235843 | missense variant | T/C;G | snv | 2.3E-03 | 35 | ||
rs1289324472 | 0.716 | 0.400 | 1 | 155236354 | missense variant | T/C | snv | 1.4E-05 | 21 | ||
rs28935197 | 0.776 | 0.280 | X | 101398942 | missense variant | T/C | snv | 5.5E-06 | 10 | ||
rs104894845 | 0.807 | 0.160 | X | 101401752 | missense variant | C/G;T | snv | 5.5E-04 | 8 | ||
rs72555392 | 0.807 | 0.200 | 3 | 33072613 | missense variant | C/T | snv | 3.6E-05 | 7 | ||
rs120074117 | 0.882 | 0.160 | 11 | 6394204 | missense variant | G/A;C;T | snv | 1.2E-05; 4.0E-06; 1.4E-04 | 5 | ||
rs28935485 | 0.925 | 0.160 | X | 101398534 | missense variant | G/C | snv | 3 | |||
rs368687817 | 1.000 | 0.120 | 17 | 42543079 | missense variant | C/T | snv | 3.3E-05 | 4.2E-05 | 2 |