| 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 | |||
| rs745738344 | 0.653 | 0.600 | 6 | 31576786 | synonymous variant | G/A | snv | 1.6E-05 | 1.4E-05 | 28 | |
| rs121913506 | 0.677 | 0.320 | 4 | 54733154 | missense variant | G/A;C;T | snv | 24 | |||
| rs1057519710 | 0.695 | 0.280 | 4 | 54733166 | missense variant | G/C;T | snv | 22 | |||
| rs80359584 | 0.807 | 0.280 | 13 | 32340757 | frameshift variant | CTTAA/- | delins | 4.2E-06 | 1.4E-05 | 8 | |
| rs3808351 | 0.827 | 0.240 | 7 | 1087023 | 5 prime UTR variant | G/A | snv | 0.29 | 7 | ||
| rs3808350 | 0.882 | 0.080 | 7 | 1086257 | intron variant | A/G;T | snv | 6 | |||
| rs7371084 | 0.925 | 0.120 | 2 | 48712814 | intron variant | T/C | snv | 0.12 | 3 | ||
| rs1355972653 | 0.882 | 0.120 | 21 | 33415009 | synonymous variant | G/A | snv | 4.0E-06 | 7.0E-06 | 3 | |
| rs9397080 | 1.000 | 0.040 | 6 | 152059380 | intron variant | C/T | snv | 0.22 | 2 | ||
| rs34777958 | 1.000 | 0.040 | 16 | 84176003 | missense variant | C/T | snv | 9.8E-03 | 1.1E-02 | 1 |