| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10115049 | 1.000 | 0.040 | 9 | 22032120 | intron variant | A/G | snv | 0.46 | 2 | ||
| rs10116277 | 0.827 | 0.160 | 9 | 22081398 | intron variant | G/T | snv | 0.62 | 8 | ||
| rs10120688 | 0.807 | 0.080 | 9 | 22056500 | intron variant | G/A | snv | 0.50 | 7 | ||
| rs10738604 | 1.000 | 0.040 | 9 | 22025494 | intron variant | G/A | snv | 0.29 | 3 | ||
| rs10757265 | 1.000 | 0.040 | 9 | 22048860 | intron variant | T/C | snv | 0.49 | 2 | ||
| rs10757267 | 1.000 | 0.040 | 9 | 22052811 | intron variant | G/A;C;T | snv | 2 | |||
| rs10757269 | 1.000 | 0.040 | 9 | 22072265 | intron variant | A/C;G | snv | 4 | |||
| rs10757270 | 1.000 | 0.040 | 9 | 22072720 | intron variant | A/C;G | snv | 0.40 | 2 | ||
| rs10811643 | 1.000 | 0.040 | 9 | 22024967 | intron variant | A/G | snv | 0.56 | 2 | ||
| rs10811645 | 1.000 | 0.040 | 9 | 22049657 | intron variant | G/A | snv | 0.59 | 2 | ||
| rs10811647 | 1.000 | 0.040 | 9 | 22065003 | intron variant | C/G;T | snv | 3 | |||
| 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 | |||
| rs10965212 | 0.925 | 0.080 | 9 | 22023796 | intron variant | T/A;C;G | snv | 3 | |||
| rs10965219 | 0.882 | 0.080 | 9 | 22053688 | intron variant | A/G | snv | 0.58 | 4 | ||
| rs10965224 | 1.000 | 0.040 | 9 | 22067277 | intron variant | T/A | snv | 0.64 | 2 | ||
| rs1333036 | 1.000 | 0.040 | 9 | 22043820 | intron variant | T/C | snv | 0.58 | 2 | ||
| rs1333037 | 0.925 | 0.040 | 9 | 22040766 | intron variant | C/T | snv | 0.71 | 3 | ||
| rs1333040 | 0.732 | 0.280 | 9 | 22083405 | intron variant | C/G;T | snv | 15 | |||
| rs1360589 | 1.000 | 0.040 | 9 | 22045318 | intron variant | C/T | snv | 0.72 | 2 | ||
| rs1360590 | 1.000 | 0.040 | 9 | 22041444 | intron variant | T/C;G | snv | 2 | |||
| rs1412829 | 0.742 | 0.400 | 9 | 22043927 | intron variant | A/G | snv | 0.28 | 14 | ||
| rs1537375 | 0.882 | 0.120 | 9 | 22116072 | intron variant | T/C;G | snv | 6 | |||
| rs1537378 | 0.882 | 0.160 | 9 | 22061615 | intron variant | A/G | snv | 0.73 | 4 | ||
| rs2069416 | 0.925 | 0.040 | 9 | 22010005 | intron variant | T/A;G | snv | 3 |