| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs775176191 | 1.000 | 0.040 | 9 | 21974745 | missense variant | A/C | snv | 1 | |||
| rs199907548 | 0.882 | 0.160 | 9 | 21974682 | missense variant | A/C;G | snv | 6.3E-04 | 2 | ||
| rs3731217 | 0.763 | 0.320 | 9 | 21984662 | intron variant | A/C;T | snv | 9 | |||
| rs104894099 | 0.851 | 0.200 | 9 | 21971183 | missense variant | A/C;T | snv | 4.6E-06 | 1 | ||
| rs3731239 | 0.763 | 0.240 | 9 | 21974219 | intron variant | A/G | snv | 0.26 | 9 | ||
| rs2811709 | 1.000 | 0.120 | 9 | 21980152 | intron variant | A/G | snv | 0.88 | 1 | ||
| rs104894098 | 0.851 | 0.200 | 9 | 21970982 | missense variant | A/T | snv | 2 | |||
| rs774904310 | 0.925 | 0.080 | 9 | 21971055 | frameshift variant | C/- | delins | 3 | |||
| rs1329443726 | 1.000 | 0.080 | 9 | 21971097 | frameshift variant | C/- | delins | 1 | |||
| rs11515 | 0.882 | 0.040 | 9 | 21968200 | 3 prime UTR variant | C/A;G | snv | 4.0E-06; 0.88 | 6 | ||
| rs1416122398 | 1.000 | 0.080 | 9 | 21974791 | missense variant | C/A;G | snv | 4.3E-06 | 1 | ||
| rs6413464 | 1.000 | 0.040 | 9 | 21970980 | missense variant | C/A;G | snv | 1.3E-03; 4.1E-06 | 1 | ||
| rs121913384 | 1.000 | 0.120 | 9 | 21971097 | stop gained | C/A;G | snv | 1 | |||
| rs3731249 | 0.683 | 0.320 | 9 | 21970917 | missense variant | C/A;G;T | snv | 2.1E-02 | 22 | ||
| rs104894094 | 0.763 | 0.200 | 9 | 21971058 | missense variant | C/A;G;T | snv | 8.5E-06; 4.3E-06 | 7 | ||
| rs104894097 | 0.807 | 0.240 | 9 | 21974757 | missense variant | C/A;G;T | snv | 1.7E-05; 1.3E-05 | 2 | ||
| rs1444669684 | 0.658 | 0.480 | 9 | 21994285 | missense variant | C/A;T | snv | 36 | |||
| rs200863613 | 0.925 | 0.080 | 9 | 21971061 | missense variant | C/A;T | snv | 8.5E-05 | 3.7E-04 | 6 | |
| rs878853646 | 0.882 | 0.080 | 9 | 21971106 | missense variant | C/A;T | snv | 4.3E-06; 8.6E-06 | 3 | ||
| rs774829510 | 0.882 | 0.040 | 9 | 21971046 | missense variant | C/A;T | snv | 3 | |||
| rs1131691186 | 0.925 | 0.120 | 9 | 21974761 | missense variant | C/A;T | snv | 2 | |||
| rs3731246 | 0.882 | 0.120 | 9 | 21971990 | intron variant | C/G | snv | 0.11 | 3 | ||
| rs45456595 | 9 | 21974641 | missense variant | C/G | snv | 2.0E-03 | 2.1E-03 | 1 | |||
| rs878853645 | 1.000 | 0.040 | 9 | 21971176 | missense variant | C/G | snv | 1 | |||
| rs104894095 | 0.827 | 0.120 | 9 | 21971200 | missense variant | C/G;T | snv | 9.0E-06 | 3 |