| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
| rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
| rs397517132 | 0.623 | 0.280 | 7 | 55191846 | missense variant | A/T | snv | 48 | |||
| rs1800734 | 0.653 | 0.400 | 3 | 36993455 | 5 prime UTR variant | G/A | snv | 0.22 | 30 | ||
| rs119456965 | 1.000 | 0.080 | 5 | 139050960 | stop gained | G/A | snv | 8.0E-06 | 7.0E-06 | 3 | |
| rs119456966 | 1.000 | 0.080 | 5 | 138947191 | stop gained | G/A | snv | 1 | |||
| rs119456967 | 1.000 | 0.080 | 5 | 138947133 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
| rs149242794 | 1.000 | 0.080 | 5 | 139051017 | missense variant | G/A | snv | 4.9E-03 | 9.7E-04 | 1 |