| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10266101 | 1.000 | 0.080 | 7 | 4034187 | intron variant | G/A;T | snv | 1 | |||
| rs10278187 | 1.000 | 0.080 | 7 | 4034741 | intron variant | C/G;T | snv | 1 | |||
| rs1031458 | 1.000 | 0.080 | 17 | 39915920 | intron variant | G/A;T | snv | 1 | |||
| rs1054037 | 1.000 | 0.080 | 4 | 102631552 | 3 prime UTR variant | C/A;T | snv | 1 | |||
| rs10982445 | 1.000 | 0.080 | 9 | 114897411 | intron variant | T/A;C | snv | 1 | |||
| rs11078929 | 1.000 | 0.080 | 17 | 39983981 | intron variant | C/G;T | snv | 1 | |||
| rs111972148 | 1.000 | 0.080 | 17 | 45895755 | intron variant | G/C;T | snv | 1 | |||
| rs11604811 | 1.000 | 0.080 | 11 | 72678939 | upstream gene variant | G/A;T | snv | 1 | |||
| rs11650661 | 1.000 | 0.080 | 17 | 39870033 | intron variant | A/C;T | snv | 1 | |||
| rs13106304 | 1.000 | 0.080 | 4 | 102633818 | intron variant | A/G;T | snv | 1 | |||
| rs13106325 | 1.000 | 0.080 | 4 | 102633835 | intron variant | A/C;G;T | snv | 1 | |||
| rs138957038 | 1.000 | 0.080 | 17 | 46002679 | intron variant | G/-;GG;GGG | delins | 1 | |||
| rs16977009 | 1.000 | 0.080 | 17 | 71920383 | intergenic variant | C/A;T | snv | 1 | |||
| rs17139244 | 1.000 | 0.080 | 16 | 6055212 | intron variant | A/G;T | snv | 1 | |||
| rs1726773 | 1.000 | 0.080 | 19 | 50424313 | intron variant | T/C;G | snv | 1 | |||
| rs1939707 | 1.000 | 0.080 | 11 | 100231366 | intron variant | C/A;G;T | snv | 1 | |||
| rs1999527 | 1.000 | 0.080 | 1 | 3339544 | intron variant | C/A;T | snv | 1 | |||
| rs2034127 | 1.000 | 0.080 | 3 | 59382348 | intron variant | A/G;T | snv | 1 | |||
| rs2034129 | 1.000 | 0.080 | 3 | 59382567 | intron variant | C/A;T | snv | 1 | |||
| rs2069235 | 1.000 | 0.080 | 22 | 39351775 | intron variant | G/A;T | snv | 1 | |||
| rs2189521 | 1.000 | 0.080 | 16 | 27402245 | 5 prime UTR variant | C/G;T | snv | 1 | |||
| rs2272695 | 1.000 | 0.080 | 4 | 102634646 | intron variant | G/C;T | snv | 1 | |||
| rs228615 | 1.000 | 0.080 | 4 | 102658303 | intron variant | A/C;T | snv | 1 | |||
| rs228616 | 1.000 | 0.080 | 4 | 102658534 | intron variant | G/A;T | snv | 1 | |||
| rs2303933 | 1.000 | 0.080 | 7 | 151069712 | intron variant | A/C;G | snv | 1 |