| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2524132 | 1.000 | 0.040 | 6 | 31297135 | intron variant | G/A;T | snv | 1 | |||
| rs2733954 | 1.000 | 0.040 | 16 | 85802650 | intron variant | T/C | snv | 0.26 | 1 | ||
| rs28362807 | 1.000 | 0.040 | 1 | 27371297 | intron variant | -/TATTTGGCC | ins | 0.32 | 1 | ||
| rs28490179 | 1.000 | 0.040 | 6 | 32551228 | upstream gene variant | C/T | snv | 0.81 | 1 | ||
| rs2951916 | 1.000 | 0.040 | 6 | 75465141 | non coding transcript exon variant | A/G | snv | 0.51 | 1 | ||
| rs295340 | 1.000 | 0.040 | 6 | 159164909 | upstream gene variant | A/G | snv | 0.53 | 1 | ||
| rs3088362 | 1.000 | 0.040 | 13 | 43859494 | intron variant | C/A;T | snv | 1 | |||
| rs3097940 | 1.000 | 0.040 | 4 | 123863618 | non coding transcript exon variant | C/T | snv | 0.48 | 1 | ||
| rs3171425 | 1.000 | 0.040 | 21 | 33296442 | 3 prime UTR variant | A/G | snv | 0.60 | 0.53 | 1 | |
| rs34411505 | 1.000 | 0.040 | 16 | 27395368 | intergenic variant | A/C;G | snv | 1 | |||
| rs3811140 | 1.000 | 0.040 | 9 | 134880265 | upstream gene variant | A/G | snv | 0.15 | 1 | ||
| rs383592 | 1.000 | 0.040 | 8 | 89792100 | downstream gene variant | C/T | snv | 0.58 | 1 | ||
| rs3856834 | 1.000 | 0.040 | 3 | 16540153 | intron variant | T/C | snv | 0.26 | 1 | ||
| rs40457 | 1.000 | 0.040 | 8 | 89811459 | intergenic variant | A/G | snv | 0.58 | 1 | ||
| rs4366152 | 1.000 | 0.040 | 9 | 114802595 | intron variant | T/C | snv | 0.75 | 1 | ||
| rs4494157 | 1.000 | 0.040 | 1 | 27370346 | intron variant | G/T | snv | 0.25 | 1 | ||
| rs4720118 | 1.000 | 0.040 | 7 | 33429629 | intron variant | T/A;C | snv | 1 | |||
| rs55894533 | 1.000 | 0.040 | 8 | 11891733 | downstream gene variant | A/C;T | snv | 1 | |||
| rs58600253 | 1.000 | 0.040 | 10 | 62748144 | intron variant | C/T | snv | 5.5E-02 | 1 | ||
| rs58744688 | 1.000 | 0.040 | 17 | 45230816 | intron variant | A/C;G | snv | 1 | |||
| rs602875 | 1.000 | 0.040 | 6 | 32605852 | intergenic variant | A/G | snv | 0.27 | 1 | ||
| rs61756401 | 1.000 | 0.040 | 15 | 89329018 | synonymous variant | C/T | snv | 4.2E-03 | 2.7E-03 | 1 | |
| rs6807915 | 1.000 | 0.040 | 3 | 12272347 | intergenic variant | T/C | snv | 0.65 | 1 | ||
| rs6863015 | 1.000 | 0.040 | 5 | 159416227 | intron variant | C/A;T | snv | 1 | |||
| rs72715458 | 1.000 | 0.040 | 4 | 180303682 | intergenic variant | G/A | snv | 0.20 | 1 |