| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1057517661 | 0.925 | 0.040 | 11 | 68685628 | missense variant | C/A;T | snv | 2 | |||
| rs4570625 | 0.724 | 0.200 | 12 | 71938143 | upstream gene variant | G/T | snv | 0.27 | 25 | ||
| rs17110747 | 0.882 | 0.120 | 12 | 72032174 | 3 prime UTR variant | G/A | snv | 0.12 | 4 | ||
| rs2302515 | 1.000 | 0.040 | 12 | 7652640 | missense variant | C/G | snv | 0.78 | 0.76 | 1 | |
| rs1867283 | 0.925 | 0.080 | 9 | 84835851 | intron variant | G/A | snv | 0.39 | 5 | ||
| rs10868235 | 0.925 | 0.040 | 9 | 84878840 | intron variant | C/T | snv | 0.40 | 6 | ||
| rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
| rs944688 | 1.000 | 0.040 | 9 | 98601678 | intron variant | C/T | snv | 0.35 | 1 |