| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11554290 | 0.583 | 0.600 | 1 | 114713908 | missense variant | T/A;C;G | snv | 25 | |||
| rs121913255 | 0.667 | 0.400 | 1 | 114713907 | missense variant | T/A;G | snv | 19 | |||
| rs121434596 | 0.677 | 0.440 | 1 | 114716123 | missense variant | C/A;G;T | snv | 4.0E-06; 4.0E-06 | 14 | ||
| rs121434595 | 0.708 | 0.320 | 1 | 114716124 | missense variant | C/A;G;T | snv | 13 | |||
| rs121913250 | 0.683 | 0.440 | 1 | 114716127 | missense variant | C/A;G;T | snv | 13 | |||
| rs121913237 | 0.611 | 0.560 | 1 | 114716126 | missense variant | C/A;G;T | snv | 8.0E-06 | 12 | ||
| rs1057519915 | 0.851 | 0.160 | 1 | 11109318 | missense variant | A/C | snv | 5 | |||
| rs1057519916 | 0.882 | 0.160 | 1 | 11109320 | missense variant | T/A | snv | 4 | |||
| rs140081212 | 0.925 | 0.080 | 1 | 155215184 | non coding transcript exon variant | G/A | snv | 2 | |||
| rs771803475 | 1.000 | 0.080 | 1 | 37761806 | missense variant | C/T | snv | 4.0E-06 | 2.8E-05 | 1 | |
| rs781375003 | 1.000 | 0.080 | 1 | 91964700 | missense variant | C/T | snv | 8.3E-06 | 7.0E-06 | 1 | |
| rs922655349 | 1.000 | 0.080 | 1 | 16131867 | missense variant | C/T | snv | 1 | |||
| rs1057519956 | 0.827 | 0.200 | 2 | 218583025 | missense variant | T/C | snv | 5 | |||
| rs1057519957 | 0.827 | 0.200 | 2 | 218583026 | missense variant | C/G | snv | 5 | |||
| rs863224846 | 0.882 | 0.160 | 2 | 157770386 | missense variant | T/C;G | snv | 4.0E-06 | 3 | ||
| rs1057519875 | 0.925 | 0.120 | 2 | 157770385 | missense variant | C/A | snv | 2 | |||
| rs1003158162 | 1.000 | 0.080 | 2 | 178531968 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs199684560 | 1.000 | 0.080 | 2 | 178633512 | missense variant | G/A | snv | 7.3E-05 | 4.2E-05 | 1 | |
| rs373526624 | 1.000 | 0.080 | 2 | 178607095 | missense variant | C/T | snv | 7.0E-04 | 1.6E-04 | 1 | |
| rs397517769 | 1.000 | 0.080 | 2 | 178542408 | missense variant | C/T | snv | 5.6E-05 | 1.4E-05 | 1 | |
| rs539470256 | 1.000 | 0.080 | 2 | 178779033 | missense variant | C/T | snv | 1.3E-04 | 7.7E-05 | 1 | |
| rs55713867 | 1.000 | 0.080 | 2 | 178575658 | missense variant | A/G | snv | 1 | |||
| rs566841339 | 1.000 | 0.080 | 2 | 219489128 | missense variant | G/A | snv | 2.8E-05 | 2.8E-05 | 1 | |
| rs756924372 | 1.000 | 0.080 | 2 | 178534461 | missense variant | G/A;C | snv | 4.0E-06 | 1 | ||
| rs757589345 | 1.000 | 0.080 | 2 | 219469198 | missense variant | G/A;C | snv | 4.0E-06 | 1 |