| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2797685 | 0.882 | 0.160 | 1 | 7819003 | intron variant | C/T | snv | 0.23 | 1 | ||
| rs2816958 | 0.827 | 0.120 | 1 | 200132792 | intron variant | A/G | snv | 0.84 | 1 | ||
| rs2902440 | 1.000 | 0.040 | 1 | 67205233 | intron variant | G/A | snv | 0.37 | 1 | ||
| rs34920465 | 0.807 | 0.160 | 1 | 22373858 | intergenic variant | A/G | snv | 0.24 | 1 | ||
| rs3806308 | 0.827 | 0.120 | 1 | 19816373 | intron variant | C/T | snv | 0.36 | 1 | ||
| rs3897478 | 1.000 | 0.040 | 1 | 119908567 | downstream gene variant | T/C | snv | 0.17 | 1 | ||
| rs4655679 | 1.000 | 0.040 | 1 | 67133974 | intron variant | C/T | snv | 0.28 | 1 | ||
| rs4656940 | 1.000 | 0.040 | 1 | 160860478 | intron variant | A/G | snv | 0.25 | 1 | ||
| rs4656958 | 0.925 | 0.040 | 1 | 160887174 | upstream gene variant | A/G;T | snv | 1 | |||
| rs4845604 | 0.776 | 0.200 | 1 | 151829204 | intron variant | G/A;C;T | snv | 1 | |||
| rs631106 | 1.000 | 0.040 | 1 | 62436136 | upstream gene variant | C/A | snv | 0.43 | 1 | ||
| rs6426833 | 0.827 | 0.120 | 1 | 19845367 | TF binding site variant | G/A | snv | 0.52 | 1 | ||
| rs6669582 | 1.000 | 0.040 | 1 | 67264372 | downstream gene variant | A/G | snv | 0.35 | 1 | ||
| rs670523 | 1.000 | 0.040 | 1 | 155908941 | intron variant | A/G | snv | 0.48 | 1 | ||
| rs7517810 | 1.000 | 0.040 | 1 | 172884320 | intron variant | C/T | snv | 0.29 | 1 | ||
| rs7518660 | 0.925 | 0.120 | 1 | 67219760 | intron variant | G/A | snv | 0.43 | 0.47 | 1 | |
| rs7539328 | 1.000 | 0.040 | 1 | 67266920 | downstream gene variant | G/A;T | snv | 1 | |||
| rs7539625 | 1.000 | 0.040 | 1 | 67207082 | intron variant | G/A | snv | 0.33 | 0.30 | 1 | |
| rs7552167 | 0.807 | 0.120 | 1 | 24192153 | upstream gene variant | A/G | snv | 0.87 | 1 | ||
| rs76418789 | 0.882 | 0.080 | 1 | 67182913 | missense variant | G/A | snv | 7.3E-03 | 4.5E-03 | 1 | |
| rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 25 | |
| rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 24 | ||
| rs780093 | 0.763 | 0.240 | 2 | 27519736 | intron variant | T/C | snv | 0.68 | 13 | ||
| rs7574865 | 0.574 | 0.720 | 2 | 191099907 | intron variant | T/G | snv | 0.79 | 8 | ||
| rs13003464 | 0.827 | 0.200 | 2 | 60959694 | intron variant | A/G | snv | 0.50 | 7 |