| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4794136 | 1.000 | 0.040 | 17 | 50356597 | synonymous variant | T/C | snv | 0.44 | 0.47 | 1 | |
| rs777761378 | 1.000 | 0.040 | 16 | 17141171 | synonymous variant | G/A | snv | 1.6E-05 | 1.4E-05 | 1 | |
| rs639752 | 0.882 | 0.120 | 11 | 102836608 | non coding transcript exon variant | C/A | snv | 0.54 | 3 | ||
| rs1799750 | 0.592 | 0.760 | 11 | 102799765 | intron variant | C/- | delins | 0.50 | 48 | ||
| rs2908004 | 1.000 | 0.040 | 7 | 121329715 | missense variant | G/A;T | snv | 0.44; 4.0E-06 | 4 | ||
| rs731236 | 0.542 | 0.760 | 12 | 47844974 | synonymous variant | A/G | snv | 0.33 | 0.34 | 81 | |
| rs2248393 | 1.000 | 0.040 | 20 | 35338300 | intron variant | C/G | snv | 0.45 | 1 | ||
| rs2626053 | 1.000 | 0.040 | 4 | 95333937 | intron variant | G/A | snv | 0.16 | 1 | ||
| rs41310883 | 1.000 | 0.040 | 1 | 151569700 | missense variant | C/G;T | snv | 8.0E-06; 1.2E-02 | 1 | ||
| rs1149620 | 1.000 | 0.040 | 11 | 76795528 | intron variant | T/A | snv | 0.50 | 1 | ||
| rs10947262 | 0.925 | 0.040 | 6 | 32405535 | non coding transcript exon variant | C/T | snv | 0.12 | 3 | ||
| rs1061622 | 0.633 | 0.760 | 1 | 12192898 | missense variant | T/G | snv | 0.22 | 0.22 | 33 | |
| rs1905786 | 1.000 | 0.040 | 8 | 118939453 | intron variant | T/A;C | snv | 2 | |||
| rs1032128 | 1.000 | 0.040 | 8 | 118939534 | intron variant | G/A | snv | 0.30 | 1 | ||
| rs1800629 | 0.472 | 0.920 | 6 | 31575254 | upstream gene variant | G/A | snv | 0.12 | 0.14 | 169 | |
| rs361525 | 0.562 | 0.760 | 6 | 31575324 | upstream gene variant | G/A | snv | 4.6E-02 | 62 | ||
| rs10502437 | 1.000 | 0.040 | 18 | 23390742 | intron variant | G/A | snv | 0.30 | 1 | ||
| rs352140 | 0.630 | 0.680 | 3 | 52222681 | synonymous variant | C/A;G;T | snv | 2.0E-05; 0.49 | 42 | ||
| rs715572 | 0.925 | 0.040 | 22 | 32838944 | intron variant | G/A | snv | 0.18 | 3 | ||
| rs1800470 | 0.515 | 0.840 | 19 | 41353016 | missense variant | G/A;C | snv | 0.55; 2.4E-04 | 107 | ||
| rs1982073 | 0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv | 32 | |||
| rs75621460 | 0.882 | 0.040 | 19 | 41327879 | intron variant | G/A | snv | 2.0E-02 | 3 | ||
| rs3771501 | 0.925 | 0.040 | 2 | 70490521 | intron variant | A/G | snv | 0.60 | 2 | ||
| rs2862851 | 1.000 | 0.040 | 2 | 70485670 | intron variant | T/C | snv | 0.58 | 1 | ||
| rs17578878 | 1.000 | 0.040 | 4 | 37899104 | intron variant | C/T | snv | 7.9E-02 | 1 |