| 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 | |
| rs116100695 | 0.925 | 0.120 | 1 | 155291918 | missense variant | G/A | snv | 3.0E-03 | 2.8E-03 | 3 | |
| rs752423472 | 0.882 | 0.160 | 1 | 155294284 | missense variant | A/C;G | snv | 4.0E-06 | 7.0E-06 | 3 | |
| rs147689373 | 0.925 | 0.160 | 1 | 155294618 | missense variant | C/T | snv | 6.9E-04 | 2.6E-03 | 2 | |
| rs201953584 | 0.925 | 0.120 | 1 | 155294726 | stop gained | C/A | snv | 4.8E-05 | 2.1E-05 | 2 | |
| rs981505482 | 1.000 | 0.120 | 1 | 155294506 | missense variant | A/G | snv | 4.0E-06 | 2.1E-05 | 2 | |
| rs1023689443 | 1.000 | 0.120 | 1 | 155293337 | missense variant | G/A | snv | 1.4E-05 | 1 | ||
| rs1035640530 | 1.000 | 0.120 | 1 | 155293526 | missense variant | G/T | snv | 1 | |||
| rs113403872 | 1.000 | 0.120 | 1 | 155291845 | missense variant | C/T | snv | 3.6E-04 | 5.1E-04 | 1 | |
| rs1167329263 | 1.000 | 0.120 | 1 | 155294341 | missense variant | C/T | snv | 1 | |||
| rs1168490341 | 1.000 | 0.120 | 1 | 155293528 | missense variant | A/T | snv | 4.0E-06 | 1.4E-05 | 1 | |
| rs118204083 | 1.000 | 0.120 | 1 | 155295457 | missense variant | G/A | snv | 1 | |||
| rs118204084 | 1.000 | 0.120 | 1 | 155293446 | missense variant | G/T | snv | 1 | |||
| rs118204085 | 1.000 | 0.120 | 1 | 155293177 | missense variant | C/T | snv | 5.2E-05 | 4.2E-05 | 1 | |
| rs118204089 | 1.000 | 0.120 | 1 | 155295555 | missense variant | G/T | snv | 1 | |||
| rs1227427396 | 1.000 | 0.120 | 1 | 155294329 | missense variant | C/G;T | snv | 7.0E-06 | 1 | ||
| rs1239029841 | 1.000 | 0.120 | 1 | 155295468 | missense variant | C/A | snv | 4.3E-06 | 7.0E-06 | 1 | |
| rs1240481888 | 1.000 | 0.120 | 1 | 155294296 | missense variant | G/T | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs1253386414 | 1.000 | 0.120 | 1 | 155294660 | missense variant | C/T | snv | 1 | |||
| rs1352610988 | 1.000 | 0.120 | 1 | 155294570 | missense variant | C/T | snv | 8.0E-06 | 1 | ||
| rs1376070580 | 1.000 | 0.120 | 1 | 155294275 | missense variant | C/T | snv | 4.0E-06 | 2.8E-05 | 1 | |
| rs138476691 | 1.000 | 0.120 | 1 | 155294358 | missense variant | G/A;T | snv | 2.6E-04; 9.2E-05 | 1 | ||
| rs138871700 | 1.000 | 0.120 | 1 | 155294276 | missense variant | G/A | snv | 2.8E-05 | 4.2E-05 | 1 | |
| rs1403323591 | 1.000 | 0.120 | 1 | 155293533 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs141560532 | 1.000 | 0.120 | 1 | 155291890 | missense variant | G/A | snv | 4.8E-05 | 4.9E-05 | 1 |