| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10738610 | 0.882 | 0.120 | 9 | 22123767 | intron variant | A/C;T | snv | 5 | |||
| rs10811650 | 0.882 | 0.200 | 9 | 22067594 | intron variant | A/G | snv | 0.37 | 5 | ||
| rs2891168 | 0.851 | 0.160 | 9 | 22098620 | intron variant | A/G | snv | 0.40 | 5 | ||
| rs3218020 | 0.882 | 0.120 | 9 | 21997873 | intron variant | G/A;C | snv | 5 | |||
| rs6475606 | 0.882 | 0.080 | 9 | 22081851 | intron variant | C/T | snv | 0.62 | 5 | ||
| rs944797 | 0.882 | 0.120 | 9 | 22115287 | intron variant | T/C;G | snv | 0.49 | 5 | ||
| rs10127775 | 1 | 230160042 | intron variant | A/G;T | snv | 4 | |||||
| rs10211524 | 2 | 64980940 | intron variant | G/A | snv | 0.51 | 4 | ||||
| rs10738607 | 0.925 | 0.080 | 9 | 22088095 | intron variant | A/G | snv | 0.42 | 4 | ||
| rs10757269 | 1.000 | 0.040 | 9 | 22072265 | intron variant | A/C;G | snv | 4 | |||
| rs10889332 | 1.000 | 0.120 | 1 | 62485187 | 3 prime UTR variant | C/T | snv | 0.39 | 4 | ||
| rs10965219 | 0.882 | 0.080 | 9 | 22053688 | intron variant | A/G | snv | 0.58 | 4 | ||
| rs1333046 | 0.925 | 0.080 | 9 | 22124124 | intron variant | T/A | snv | 0.43 | 4 | ||
| rs1440581 | 1.000 | 0.080 | 4 | 88305270 | intron variant | T/A;C | snv | 4 | |||
| rs1537378 | 0.882 | 0.160 | 9 | 22061615 | intron variant | A/G | snv | 0.73 | 4 | ||
| rs1912826 | 4 | 186228386 | intron variant | G/A;C | snv | 4 | |||||
| rs2657880 | 12 | 56469986 | 3 prime UTR variant | G/C | snv | 0.15 | 4 | ||||
| rs615552 | 0.925 | 0.120 | 9 | 22026078 | intron variant | T/C | snv | 0.29 | 4 | ||
| rs7857345 | 0.925 | 0.080 | 9 | 22087474 | non coding transcript exon variant | T/A;C | snv | 4 | |||
| rs944801 | 0.882 | 0.120 | 9 | 22051671 | intron variant | G/A;C | snv | 4 | |||
| rs1004638 | 1.000 | 0.040 | 9 | 22115590 | intron variant | A/C;T | snv | 3 | |||
| rs10733376 | 1.000 | 0.080 | 9 | 22114470 | intron variant | G/C | snv | 0.64 | 3 | ||
| rs10738604 | 1.000 | 0.040 | 9 | 22025494 | intron variant | G/A | snv | 0.29 | 3 | ||
| rs10738605 | 0.925 | 0.120 | 9 | 22049131 | non coding transcript exon variant | C/A;G | snv | 3 | |||
| rs10738609 | 1.000 | 0.040 | 9 | 22114496 | intron variant | A/C;G;T | snv | 3 |