| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7028570 | 1.000 | 0.040 | 9 | 22048684 | intron variant | G/A | snv | 0.50 | 2 | ||
| rs10757265 | 1.000 | 0.040 | 9 | 22048860 | intron variant | T/C | snv | 0.49 | 2 | ||
| rs10738605 | 0.925 | 0.120 | 9 | 22049131 | non coding transcript exon variant | C/A;G | snv | 3 | |||
| rs10811645 | 1.000 | 0.040 | 9 | 22049657 | intron variant | G/A | snv | 0.59 | 2 | ||
| rs944799 | 1.000 | 0.040 | 9 | 22050614 | intron variant | A/G | snv | 0.50 | 2 | ||
| rs944801 | 0.882 | 0.120 | 9 | 22051671 | intron variant | G/A;C | snv | 4 | |||
| rs6475604 | 0.925 | 0.040 | 9 | 22052735 | intron variant | T/C | snv | 0.72 | 3 | ||
| rs10757267 | 1.000 | 0.040 | 9 | 22052811 | intron variant | G/A;C;T | snv | 2 | |||
| rs10965219 | 0.882 | 0.080 | 9 | 22053688 | intron variant | A/G | snv | 0.58 | 4 | ||
| rs7027048 | 1.000 | 0.040 | 9 | 22053710 | intron variant | A/G;T | snv | 2 | |||
| rs7030641 | 1.000 | 0.040 | 9 | 22054041 | intron variant | C/T | snv | 0.72 | 2 | ||
| rs2383204 | 0.827 | 0.160 | 9 | 22055049 | intron variant | A/G;T | snv | 6 | |||
| rs7866783 | 1.000 | 0.040 | 9 | 22056360 | non coding transcript exon variant | A/G | snv | 0.71 | 2 | ||
| rs10120688 | 0.807 | 0.080 | 9 | 22056500 | intron variant | G/A | snv | 0.50 | 7 | ||
| rs2383205 | 0.925 | 0.080 | 9 | 22060936 | intron variant | A/C;G | snv | 3 | |||
| rs2184061 | 1.000 | 0.040 | 9 | 22061563 | intron variant | C/A;T | snv | 0.64 | 2 | ||
| rs1537378 | 0.882 | 0.160 | 9 | 22061615 | intron variant | A/G | snv | 0.73 | 4 | ||
| rs8181050 | 1.000 | 0.040 | 9 | 22064392 | intron variant | G/A;C;T | snv | 2 | |||
| rs10811647 | 1.000 | 0.040 | 9 | 22065003 | intron variant | C/G;T | snv | 3 | |||
| rs1333039 | 1.000 | 0.040 | 9 | 22065658 | splice region variant | G/A;C;T | snv | 2 | |||
| rs10965224 | 1.000 | 0.040 | 9 | 22067277 | intron variant | T/A | snv | 0.64 | 2 | ||
| rs10811650 | 0.882 | 0.200 | 9 | 22067594 | intron variant | A/G | snv | 0.37 | 5 | ||
| rs10811651 | 1.000 | 0.040 | 9 | 22067831 | intron variant | G/A;C | snv | 2 | |||
| rs4977756 | 0.683 | 0.440 | 9 | 22068653 | intron variant | G/A | snv | 0.64 | 24 | ||
| rs4451405 | 9 | 22071751 | intron variant | C/T | snv | 0.69 | 1 |