Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs267607641 | 1.000 | 0.120 | 1 | 156135188 | missense variant | T/C | snv | 1 | |||
| rs267607642 | 1.000 | 0.120 | 1 | 156136921 | missense variant | G/T | snv | 8.0E-06 | 1 | ||
| rs267607643 | 1.000 | 0.120 | 1 | 156134455 | missense variant | GG/CC | mnv | 1 | |||
| rs56694480 | 1.000 | 0.120 | 1 | 156115021 | missense variant | C/G | snv | 1 | |||
| rs56699480 | 1.000 | 0.120 | 1 | 156137017 | stop gained | C/T | snv | 1 | |||
| rs57048196 | 1.000 | 0.120 | 1 | 156134965 | missense variant | A/G | snv | 1 | |||
| rs57394692 | 1.000 | 0.120 | 1 | 156136946 | missense variant | T/C | snv | 1 | |||
| rs57793737 | 1.000 | 0.120 | 1 | 156115106 | missense variant | T/A;C;G | snv | 1 | |||
| rs58105277 | 1.000 | 0.120 | 1 | 156135971 | missense variant | G/A | snv | 2.8E-05 | 1 | ||
| rs58541611 | 1.000 | 0.120 | 1 | 156136393 | missense variant | A/G;T | snv | 1 | |||
| rs59931416 | 1.000 | 0.120 | 1 | 156115066 | missense variant | C/A;T | snv | 1 | |||
| rs60446065 | 1.000 | 0.120 | 1 | 156115045 | missense variant | G/A | snv | 1 | |||
| rs60992550 | 1.000 | 0.120 | 1 | 156136423 | missense variant | A/T | snv | 1 | |||
| rs61177390 | 1.000 | 0.120 | 1 | 156135992 | missense variant | G/A | snv | 3.6E-05 | 2.8E-05 | 1 | |
| rs61235244 | 1.000 | 0.120 | 1 | 156136424 | missense variant | C/A | snv | 1 | |||
| rs61527854 | 1.000 | 0.120 | 1 | 156135283 | missense variant | T/C | snv | 1 | |||
| rs61578124 | 1.000 | 0.120 | 1 | 156114992 | missense variant | G/C;T | snv | 5.4E-05 | 1 | ||
| rs61616775 | 1.000 | 0.120 | 1 | 156135257 | missense variant | A/C | snv | 1 | |||
| rs58034145 | 0.827 | 0.160 | 1 | 156134830 | missense variant | A/C | snv | 10 | |||
| rs57983345 | 0.851 | 0.160 | 1 | 156115034 | missense variant | A/G | snv | 6 | |||
| rs61195471 | 0.827 | 0.160 | 1 | 156134496 | missense variant | G/A | snv | 6 | |||
| rs59332535 | 0.827 | 0.160 | 1 | 156134911 | missense variant | G/A | snv | 5 | |||
| rs61444459 | 0.851 | 0.160 | 1 | 156137667 | missense variant | G/A;C | snv | 5 | |||
| rs267607571 | 0.882 | 0.160 | 1 | 156134458 | missense variant | G/A;T | snv | 4 | |||
| rs28933091 | 0.882 | 0.160 | 1 | 156134474 | missense variant | C/A;G | snv | 4 |