| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4771856 | 1.000 | 0.080 | 13 | 92342256 | intron variant | C/A | snv | 0.29 | 1 | ||
| rs7982677 | 1.000 | 0.080 | 13 | 92336070 | intron variant | C/A | snv | 0.29 | 1 | ||
| rs804280 | 0.882 | 0.120 | 8 | 11755189 | intron variant | C/A;G | snv | 6 | |||
| rs115099192 | 0.827 | 0.080 | 8 | 11758366 | missense variant | C/A;G | snv | 5.1E-04; 6.8E-05 | 5 | ||
| rs145895196 | 0.925 | 0.120 | 20 | 10641566 | missense variant | C/A;T | snv | 1.6E-05; 1.9E-03 | 2 | ||
| rs115875978 | 1.000 | 0.080 | 15 | 58010691 | missense variant | C/A;T | snv | 5.9E-04; 4.0E-06 | 1 | ||
| rs121434424 | 1.000 | 0.080 | 19 | 18869231 | missense variant | C/A;T | snv | 2.1E-04 | 1 | ||
| rs1448468136 | 1.000 | 0.080 | 8 | 105802610 | missense variant | C/A;T | snv | 1 | |||
| rs2010963 | 0.542 | 0.840 | 6 | 43770613 | 5 prime UTR variant | C/G | snv | 0.68 | 82 | ||
| rs104893904 | 0.807 | 0.160 | 5 | 173235023 | missense variant | C/G | snv | 1.1E-03 | 7.1E-04 | 6 | |
| rs387906814 | 1.000 | 0.080 | 18 | 22171736 | missense variant | C/G | snv | 6.6E-05 | 6.7E-04 | 1 | |
| rs833061 | 0.605 | 0.600 | 6 | 43769749 | upstream gene variant | C/G;T | snv | 42 | |||
| rs774966208 | 1.000 | 0.080 | 9 | 136523014 | missense variant | C/G;T | snv | 1 | |||
| rs3025039 | 0.576 | 0.720 | 6 | 43784799 | 3 prime UTR variant | C/T | snv | 0.13 | 62 | ||
| rs653178 | 0.672 | 0.600 | 12 | 111569952 | intron variant | C/T | snv | 0.67 | 41 | ||
| rs587783446 | 0.763 | 0.280 | 8 | 60850546 | stop gained | C/T | snv | 19 | |||
| rs387906769 | 0.807 | 0.080 | 8 | 11708799 | missense variant | C/T | snv | 7.3E-05 | 4.2E-05 | 7 | |
| rs28939668 | 0.807 | 0.200 | 20 | 10652533 | missense variant | C/T | snv | 6 | |||
| rs17153694 | 0.851 | 0.160 | 8 | 11730972 | intron variant | C/T | snv | 0.12 | 4 | ||
| rs121918351 | 0.882 | 0.240 | 20 | 10658611 | missense variant | C/T | snv | 3 | |||
| rs2228638 | 1.000 | 0.080 | 10 | 33186354 | missense variant | C/T | snv | 0.12 | 9.4E-02 | 3 | |
| rs387906818 | 0.882 | 0.120 | 18 | 22181516 | missense variant | C/T | snv | 3 | |||
| rs233716 | 1.000 | 0.080 | 12 | 112602139 | intron variant | C/T | snv | 0.58 | 1 | ||
| rs771792843 | 1.000 | 0.080 | 8 | 11749060 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs1554034812 | 0.925 | 0.240 | 5 | 37058938 | frameshift variant | G/- | delins | 3 |