| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs114925667 | 0.672 | 0.520 | 3 | 132675903 | missense variant | G/A;T | snv | 1.9E-03; 4.1E-06 | 64 | ||
| rs1553770577 | 0.724 | 0.480 | 3 | 132675342 | missense variant | T/C | snv | 37 | |||
| rs374052333 | 0.763 | 0.320 | 3 | 132671032 | stop gained | C/G;T | snv | 4.0E-06 | 27 | ||
| rs745968949 | 1.000 | 3 | 132675290 | stop gained | C/A;T | snv | 4.0E-06 | 1 | |||
| rs886039757 | 1.000 | 3 | 132675339 | stop gained | C/T | snv | 1 | ||||
| rs886039759 | 1.000 | 3 | 132672143 | missense variant | G/A | snv | 4.0E-06 | 1 | |||
| rs532178791 | 1.000 | 3 | 132665830 | start lost | A/G | snv | 1.0E-04 | 1.4E-05 | 1 | ||
| rs772888455 | 1.000 | 3 | 132675345 | missense variant | G/A | snv | 4.0E-06 | 1 | |||
| rs774318611 | 1.000 | 3 | 132665825 | missense variant | G/A | snv | 1 | ||||
| rs886039756 | 1.000 | 3 | 132665842 | stop gained | C/T | snv | 7.0E-06 | 1 | |||
| rs886039758 | 1.000 | 3 | 132675627 | frameshift variant | -/C | ins | 1 | ||||
| rs886039760 | 1.000 | 3 | 132676476 | missense variant | G/T | snv | 1 | ||||
| rs886039761 | 1.000 | 3 | 132670973 | missense variant | G/A | snv | 1 |