| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1556516 | 9 | 22100177 | intron variant | G/A;C | snv | 1 | |||||
| rs17404667 | 3 | 64288876 | intron variant | C/G | snv | 6.2E-02 | 1 | ||||
| rs1851024 | 4 | 71842104 | intergenic variant | G/A | snv | 0.93 | 1 | ||||
| rs188234402 | 9 | 22029058 | intron variant | T/A | snv | 2.1E-05 | 1 | ||||
| rs1998013 | 1 | 55492357 | intron variant | C/T | snv | 4.4E-03 | 1 | ||||
| rs201049435 | 9 | 22029059 | intron variant | AA/-;A;AAA;AAAA | delins | 6.9E-03 | 1 | ||||
| rs2168889 | 4 | 74357994 | intergenic variant | A/G | snv | 4.7E-02 | 1 | ||||
| rs2306786 | 15 | 59195731 | intron variant | C/G | snv | 8.0E-02 | 1 | ||||
| rs2390582 | 1 | 90478350 | intergenic variant | A/G | snv | 0.15 | 1 | ||||
| rs34059530 | 9 | 22029059 | intron variant | AA/-;A;AAA;AAAA | delins | 1 | |||||
| rs397733626 | 9 | 22029059 | intron variant | AA/-;A;AAA;AAAA | delins | 0.58 | 1 | ||||
| rs4451405 | 9 | 22071751 | intron variant | C/T | snv | 0.69 | 1 | ||||
| rs4711863 | 6 | 12915185 | intron variant | G/C | snv | 0.29 | 1 | ||||
| rs565448157 | 9 | 22029059 | intron variant | AA/-;A;AAA;AAAA | delins | 8.0E-04 | 1 | ||||
| rs616082 | 18 | 31787677 | intergenic variant | C/A;T | snv | 1 | |||||
| rs7092929 | 10 | 3496602 | splice region variant | A/C;T | snv | 1 | |||||
| rs7341791 | 9 | 22112428 | intron variant | A/G | snv | 0.65 | 1 | ||||
| rs741013 | 3 | 64306961 | intron variant | A/T | snv | 6.0E-02 | 1 | ||||
| rs749924 | 2 | 242084344 | upstream gene variant | C/T | snv | 0.25 | 1 | ||||
| rs7857118 | 9 | 22124141 | intron variant | A/T | snv | 0.64 | 1 | ||||
| rs8089491 | 18 | 31763291 | upstream gene variant | G/A | snv | 5.4E-02 | 1 | ||||
| rs4810479 | 1.000 | 0.040 | 20 | 45916409 | upstream gene variant | C/T | snv | 0.68 | 7 | ||
| rs10757269 | 1.000 | 0.040 | 9 | 22072265 | intron variant | A/C;G | snv | 4 | |||
| rs1303 | 0.925 | 0.040 | 14 | 94378506 | missense variant | T/G | snv | 0.28 | 0.22 | 4 | |
| rs1004638 | 1.000 | 0.040 | 9 | 22115590 | intron variant | A/C;T | snv | 3 |