Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs60682848 | 0.790 | 0.200 | 1 | 156134838 | stop gained | C/T | snv | 7.0E-06 | 11 | ||
rs572010627 | 0.851 | 0.160 | 1 | 161306738 | missense variant | A/C;T | snv | 8.0E-06 | 4 | ||
rs1553259662 | 0.827 | 0.200 | 1 | 161306821 | missense variant | A/G | snv | 7 | |||
rs62636495 | 0.925 | 0.200 | 2 | 219418500 | missense variant | C/A;T | snv | 4 | |||
rs374528680 | 0.851 | 0.240 | 12 | 2686216 | missense variant | G/A;C | snv | 4.0E-06; 6.0E-05 | 5 | ||
rs6795970 | 0.807 | 0.200 | 3 | 38725184 | missense variant | A/G | snv | 0.65 | 0.70 | 13 | |
rs587782958 | 0.790 | 0.120 | 11 | 47333552 | splice region variant | C/T | snv | 1.7E-05 | 10 |