| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2515475 | 1.000 | 0.040 | 8 | 6530918 | intron variant | C/T | snv | 0.19 | 1 | ||
| rs78142040 | 1.000 | 0.040 | X | 2914730 | non coding transcript exon variant | C/T | snv | 1 | |||
| rs13402990 | 1.000 | 0.040 | 2 | 70231632 | intron variant | A/T | snv | 9.7E-03 | 1 | ||
| rs2592178 | 1.000 | 0.040 | 2 | 70245350 | intron variant | G/A | snv | 0.27 | 1 | ||
| rs10905928 | 1.000 | 0.040 | 10 | 11300924 | intron variant | C/A | snv | 0.21 | 1 | ||
| rs2277212 | 1.000 | 0.040 | 10 | 11257772 | synonymous variant | A/T | snv | 0.75 | 0.74 | 1 | |
| rs7068124 | 1.000 | 0.040 | 10 | 11023453 | intron variant | T/C;G | snv | 1 | |||
| rs3814634 | 1.000 | 0.040 | 10 | 11099442 | splice region variant | G/T | snv | 0.37 | 1 | ||
| rs2298991 | 1.000 | 0.040 | 4 | 109970856 | intron variant | T/A;G | snv | 1 | |||
| rs4698803 | 1.000 | 0.040 | 4 | 109993271 | missense variant | A/G;T | snv | 0.85 | 1 | ||
| rs6533485 | 1.000 | 0.040 | 4 | 110006407 | intron variant | G/C | snv | 0.61 | 1 | ||
| rs516651 | 1.000 | 0.040 | 1 | 231406910 | intron variant | C/T | snv | 0.15 | 1 | ||
| rs782230926 | 1.000 | 0.040 | 17 | 41734538 | missense variant | G/T | snv | 8.4E-06 | 7.0E-06 | 1 | |
| rs672961 | 1.000 | 0.040 | 1 | 70101505 | intron variant | C/G | snv | 0.99 | 1 | ||
| rs151139112 | 1.000 | 0.040 | 12 | 120322275 | missense variant | C/T | snv | 8.9E-04 | 3.2E-03 | 1 | |
| rs34568801 | 1.000 | 0.040 | 1 | 19975708 | missense variant | C/T | snv | 4.6E-03 | 4.3E-03 | 1 | |
| rs1190286 | 1.000 | 0.040 | 6 | 105163071 | intron variant | C/T | snv | 0.66 | 1 | ||
| rs9605146 | 1.000 | 0.040 | 22 | 16784304 | missense variant | G/A | snv | 0.39 | 1 | ||
| rs3848719 | 1.000 | 0.040 | 20 | 45967906 | synonymous variant | G/A | snv | 0.33 | 0.32 | 1 | |
| rs7692976 | 1.000 | 0.040 | 4 | 109990411 | intron variant | A/G;T | snv | 2 | |||
| rs832582 | 0.925 | 0.080 | 5 | 56881916 | missense variant | G/A | snv | 0.76 | 0.78 | 2 | |
| rs1042689672 | 0.925 | 0.080 | 10 | 79557504 | missense variant | A/G | snv | 7.0E-06 | 2 | ||
| rs146709251 | 0.882 | 0.080 | 16 | 2279070 | missense variant | G/A | snv | 4.3E-03 | 3.0E-03 | 3 | |
| rs7022797 | 0.882 | 0.120 | 9 | 88989548 | upstream gene variant | T/G | snv | 0.38 | 3 | ||
| rs761495176 | 0.882 | 0.080 | 5 | 143400263 | missense variant | T/C | snv | 1.7E-05 | 3 |