Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10517480 | 4 | 59883111 | intergenic variant | A/T | snv | 0.27 | 2 | ||||
rs108499 | 11 | 61779765 | intron variant | C/T | snv | 0.27 | 2 | ||||
rs1109748 | 11 | 61955173 | synonymous variant | C/A | snv | 0.21 | 0.11 | 2 | |||
rs11230815 | 11 | 61868654 | downstream gene variant | G/C;T | snv | 2 | |||||
rs149803 | 11 | 61771548 | synonymous variant | C/G;T | snv | 0.18 | 2 | ||||
rs17156426 | 11 | 61841851 | intron variant | A/G;T | snv | 2 | |||||
rs17156442 | 11 | 61846551 | intron variant | C/T | snv | 0.11 | 2 | ||||
rs174449 | 11 | 61872907 | downstream gene variant | G/A | snv | 0.54 | 2 | ||||
rs174456 | 11 | 61888710 | intron variant | C/A | snv | 0.59 | 2 | ||||
rs174464 | 11 | 61890454 | intron variant | A/G | snv | 0.59 | 2 | ||||
rs174468 | 11 | 61896219 | upstream gene variant | G/A | snv | 0.28 | 2 | ||||
rs174472 | 11 | 61904484 | intron variant | A/G | snv | 0.41 | 2 | ||||
rs174476 | 11 | 61906646 | synonymous variant | C/A;G;T | snv | 0.30 | 2 | ||||
rs174478 | 11 | 61911104 | intron variant | T/G | snv | 0.31 | 2 | ||||
rs174479 | 11 | 61911282 | intron variant | C/G | snv | 0.17 | 2 | ||||
rs174532 | 11 | 61781402 | intron variant | G/A | snv | 0.20 | 2 | ||||
rs174579 | 11 | 61838141 | intron variant | C/T | snv | 0.16 | 2 | ||||
rs174585 | 11 | 61844222 | intron variant | G/A;T | snv | 2 | |||||
rs174591 | 11 | 61850204 | intron variant | T/A;G | snv | 2 | |||||
rs174593 | 11 | 61851359 | intron variant | T/C | snv | 0.24 | 2 | ||||
rs174597 | 11 | 61853568 | intron variant | G/A;C;T | snv | 2 | |||||
rs174605 | 11 | 61859449 | intron variant | G/T | snv | 0.20 | 2 | ||||
rs174611 | 11 | 61860409 | intron variant | T/C | snv | 0.21 | 2 | ||||
rs174626 | 11 | 61869585 | downstream gene variant | G/A | snv | 0.48 | 2 | ||||
rs174634 | 11 | 61879915 | intron variant | G/C;T | snv | 2 |