Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
rs75932628 | 0.662 | 0.480 | 6 | 41161514 | missense variant | C/A;T | snv | 6.8E-05; 2.6E-03 | 28 | ||
rs7120118 | 0.716 | 0.360 | 11 | 47264739 | intron variant | T/C | snv | 0.38 | 18 | ||
rs200161705 | 0.882 | 0.160 | 4 | 169585374 | missense variant | C/A;T | snv | 6.0E-05; 2.3E-03 | 5 | ||
rs1272951905 | 0.925 | 0.160 | 16 | 86532210 | missense variant | C/T | snv | 2.1E-05 | 3 | ||
rs771845093 | 0.925 | 0.160 | 1 | 12005903 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 3 |