Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs396991 | 0.742 | 0.480 | 1 | 161544752 | missense variant | A/C;G;T | snv | 0.33; 4.1E-06 | 14 | ||
rs587782329 | 0.677 | 0.280 | 17 | 7674217 | missense variant | C/A;G;T | snv | 23 | |||
rs730882025 | 0.724 | 0.360 | 17 | 7674885 | missense variant | C/A;G;T | snv | 21 | |||
rs1305324490 | 17 | 7673738 | missense variant | C/G | snv | 4.0E-06 | 1 | ||||
rs672601296 | 17 | 7673734 | missense variant | G/A | snv | 1 | |||||
rs863224683 | 17 | 7675224 | missense variant | G/A;C | snv | 4 | |||||
rs144340710 | 1.000 | 0.120 | 17 | 7674259 | missense variant | T/A;C | snv | 4.0E-06; 1.8E-04 | 2 | ||
rs1000256867 | 17 | 7673550 | missense variant | T/A;G | snv | 4.0E-06 | 1 |