Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121918497 | 0.776 | 0.160 | 10 | 121520052 | missense variant | T/G | snv | 3 | |||
rs1057519036 | 0.925 | 0.080 | 10 | 121520092 | missense variant | A/C | snv | 2 | |||
rs121913477 | 1.000 | 0.120 | 10 | 121515289 | missense variant | G/C;T | snv | 2 | |||
rs121918499 | 0.925 | 0.160 | 10 | 121520048 | missense variant | C/A;G | snv | 2 | |||
rs879253721 | 0.925 | 0.080 | 10 | 121517316 | splice region variant | T/C | snv | 2 | |||
rs1057519041 | 0.925 | 0.160 | 10 | 121517465 | splice acceptor variant | T/C | snv | 2 | |||
rs121918492 | 0.882 | 0.080 | 10 | 121517372 | missense variant | G/C | snv | 7.0E-06 | 2 | ||
rs121918507 | 0.882 | 0.280 | 10 | 121498591 | missense variant | T/C | snv | 2 | |||
rs777169135 | 0.851 | 0.080 | 10 | 121488064 | missense variant | T/C;G | snv | 4.0E-06 | 1 | ||
rs1057520044 | 1.000 | 0.080 | 10 | 121498597 | missense variant | T/C | snv | 1 | |||
rs121913475 | 10 | 121519989 | missense variant | T/C | snv | 1 | |||||
rs1057520028 | 10 | 121515283 | missense variant | T/C | snv | 1 | |||||
rs1057520029 | 0.925 | 0.120 | 10 | 121488003 | missense variant | T/A | snv | 1 | |||
rs1057520027 | 10 | 121488005 | missense variant | T/C | snv | 1 | |||||
rs1057519791 | 1.000 | 0.080 | 10 | 121518810 | missense variant | G/C | snv | 1 | |||
rs1057519047 | 1.000 | 0.080 | 10 | 121488055 | missense variant | T/C;G | snv | 1 | |||
rs879253719 | 1.000 | 0.080 | 10 | 121517464 | splice acceptor variant | C/T | snv | 1 | |||
rs1358919643 | 1.000 | 0.080 | 10 | 121517463 | missense variant | C/A;T | snv | 4.0E-06 | 1 | ||
rs121918495 | 0.925 | 0.080 | 10 | 121517382 | missense variant | T/G | snv | 1 | |||
rs121918510 | 1.000 | 0.080 | 10 | 121517441 | missense variant | T/G | snv | 1 | |||
rs121918509 | 1.000 | 0.280 | 10 | 121488095 | missense variant | C/T | snv | 1 | |||
rs121918508 | 0.851 | 0.360 | 10 | 121488035 | missense variant | C/T | snv | 1 | |||
rs1554917471 | 1.000 | 0.280 | 10 | 121500910 | missense variant | C/A | snv | 1 | |||
rs1554907337 | 1.000 | 0.280 | 10 | 121487390 | missense variant | G/A | snv | 1 | |||
rs1057519799 | 1.000 | 10 | 121498556 | missense variant | C/A;G;T | snv | 1 |