Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519877 | 0.763 | 0.280 | 15 | 44711549 | start lost | G/A | snv | 10 | |||
rs1023835002 | 0.763 | 0.280 | 15 | 44711547 | start lost | A/G;T | snv | 10 | |||
rs1057519879 | 0.763 | 0.280 | 15 | 44711548 | start lost | T/C;G | snv | 10 | |||
rs863225287 | 1.000 | 0.080 | 15 | 44711614 | splice donor variant | G/T | snv | 1 | |||
rs752734259 | 1.000 | 15 | 44672114 | stop gained | A/G;T | snv | 6.5E-06 | 7.0E-06 | 1 | ||
rs1555385717 | 1.000 | 15 | 44668978 | splice donor variant | A/G | snv | 1 | ||||
rs1361024832 | 1.000 | 15 | 44672023 | missense variant | A/T | snv | 6.5E-06 | 1 | |||
rs548527219 | 1.000 | 15 | 44672425 | stop gained | G/A | snv | 3.2E-05 | 2.8E-05 | 1 | ||
rs1351320025 | 1.000 | 15 | 44669869 | stop gained | G/A | snv | 1 | ||||
rs1156737044 | 1.000 | 15 | 44672106 | missense variant | A/C | snv | 6.5E-06 | 1 | |||
rs104894481 | 1.000 | 0.080 | 15 | 44711577 | missense variant | G/C;T | snv | 4.0E-06 | 1 |