| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1106357 | 1 | 21490592 | intergenic variant | C/T | snv | 0.37 | 3 | ||||
| rs1697421 | 1 | 21496799 | intergenic variant | C/A;T | snv | 3 | |||||
| rs4654748 | 1.000 | 0.040 | 1 | 21459575 | intron variant | C/T | snv | 0.38 | 3 | ||
| rs1256335 | 1 | 21563893 | intron variant | G/A | snv | 0.80 | 2 | ||||
| rs4654932 | 1 | 21425060 | intron variant | G/A;C | snv | 2 | |||||
| rs12132412 | 1 | 21493549 | intergenic variant | A/C;G | snv | 1 | |||||
| rs2267739 | 7 | 31097283 | intron variant | C/G;T | snv | 1 | |||||
| rs1772719 | 1 | 21577881 | 3 prime UTR variant | A/C | snv | 0.19 | 1 | ||||
| rs28789220 | 15 | 66988590 | intron variant | G/C | snv | 0.14 | 1 | ||||
| rs12118362 | 1 | 21445504 | intron variant | G/A;C | snv | 1 | |||||
| rs10056527 | 5 | 124740390 | intron variant | C/T | snv | 0.19 | 1 |