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 | |
rs1001179 | 0.641 | 0.680 | 11 | 34438684 | upstream gene variant | C/T | snv | 0.16 | 33 | ||
rs9653711 | 0.851 | 0.120 | 21 | 33029641 | intron variant | G/A;C | snv | 4 | |||
rs6517137 | 0.882 | 0.120 | 21 | 33028471 | 3 prime UTR variant | T/C | snv | 0.11 | 3 | ||
rs1005573 | 0.925 | 0.080 | 21 | 33026408 | 5 prime UTR variant | C/T | snv | 0.73 | 2 | ||
rs1217401 | 0.925 | 0.080 | 1 | 113896329 | missense variant | A/G | snv | 0.30 | 0.42 | 2 | |
rs6517135 | 0.925 | 0.080 | 21 | 33025263 | intron variant | T/C | snv | 0.33 | 2 |