Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913500 | 0.529 | 0.600 | 2 | 208248388 | missense variant | C/A;G;T | snv | 4.0E-06 | 96 | ||
rs118101777 | 0.614 | 0.280 | 15 | 90087472 | missense variant | C/T | snv | 2.0E-03 | 1.6E-03 | 42 | |
rs55819519 | 0.627 | 0.400 | 17 | 7673751 | missense variant | C/A;G;T | snv | 1.6E-04 | 1.3E-04 | 40 | |
rs28934575 | 0.641 | 0.400 | 17 | 7674230 | missense variant | C/A;G;T | snv | 37 | |||
rs28934574 | 0.658 | 0.440 | 17 | 7673776 | missense variant | G/A;C | snv | 4.0E-06 | 31 | ||
rs1057519903 | 0.683 | 0.080 | 1 | 226064434 | missense variant | A/T | snv | 28 | |||
rs6010620 | 0.701 | 0.360 | 20 | 63678486 | intron variant | A/C;G | snv | 21 | |||
rs1412829 | 0.742 | 0.400 | 9 | 22043927 | intron variant | A/G | snv | 0.28 | 14 | ||
rs760090729 | 0.851 | 0.040 | 6 | 27810468 | missense variant | G/A | snv | 4 | |||
rs866960721 | 0.851 | 0.040 | 6 | 26196856 | missense variant | C/G;T | snv | 4.0E-06 | 4 | ||
rs1415342243 | 0.851 | 0.040 | 6 | 26225549 | missense variant | G/A | snv | 4.0E-06 | 4 | ||
rs751859698 | 0.925 | 0.040 | 1 | 75898031 | missense variant | T/A;C | snv | 1.2E-05 | 2 |