| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1889891 | 1.000 | 0.040 | 6 | 129492201 | non coding transcript exon variant | C/T | snv | 0.37 | 1 | ||
| rs2808510 | 1.000 | 0.040 | 1 | 200366947 | non coding transcript exon variant | C/T | snv | 0.29 | 1 | ||
| rs2342406 | 1.000 | 0.040 | 2 | 44925609 | intron variant | T/C | snv | 0.19 | 1 | ||
| rs5742629 | 1.000 | 0.040 | 12 | 102463485 | non coding transcript exon variant | T/C | snv | 0.32 | 1 | ||
| rs9321170 | 1.000 | 0.040 | 6 | 129501692 | intron variant | G/A;C | snv | 1 | |||
| rs2181346 | 1.000 | 0.040 | 14 | 54085710 | regulatory region variant | A/T | snv | 0.23 | 1 | ||
| rs10511652 | 1.000 | 0.040 | 9 | 18362867 | intron variant | A/G | snv | 0.54 | 1 | ||
| rs34217772 | 1.000 | 0.040 | 14 | 41804367 | intron variant | C/G | snv | 0.16 | 1 | ||
| rs11606250 | 1.000 | 0.040 | 11 | 40127750 | intron variant | G/A | snv | 0.17 | 1 | ||
| rs11218544 | 1.000 | 0.040 | 11 | 122168344 | intron variant | T/G | snv | 0.15 | 1 | ||
| rs10488 | 1.000 | 0.040 | 11 | 102797291 | synonymous variant | C/G;T | snv | 4.0E-06; 5.7E-02 | 1 | ||
| rs12965607 | 1.000 | 0.040 | 18 | 49864655 | intron variant | T/G | snv | 1.0E-01 | 1 | ||
| rs479445 | 1.000 | 0.040 | 1 | 60875960 | intron variant | T/A | snv | 0.31 | 1 | ||
| rs1793639 | 1.000 | 0.040 | 11 | 132061637 | intron variant | G/A | snv | 0.39 | 1 | ||
| rs13129838 | 1.000 | 0.040 | 4 | 79587634 | non coding transcript exon variant | T/C | snv | 0.66 | 1 | ||
| rs2071754 | 1.000 | 0.040 | 11 | 31791034 | non coding transcript exon variant | C/G;T | snv | 1 | |||
| rs2799081 | 1.000 | 0.040 | 6 | 28302807 | downstream gene variant | T/C | snv | 0.41 | 1 | ||
| rs1550094 | 1.000 | 0.040 | 2 | 232520686 | missense variant | G/A | snv | 0.72 | 0.64 | 1 | |
| rs1550870 | 1.000 | 0.040 | 11 | 18729494 | synonymous variant | C/T | snv | 0.39 | 0.41 | 1 | |
| rs7968679 | 1.000 | 0.040 | 12 | 9160708 | intron variant | A/C;G | snv | 1 | |||
| rs13380104 | 1.000 | 0.040 | 15 | 79086479 | intron variant | C/T | snv | 0.43 | 1 | ||
| rs10887265 | 1.000 | 0.040 | 10 | 84255817 | intron variant | G/C | snv | 0.48 | 1 | ||
| rs12603825 | 1.000 | 0.040 | 17 | 1770111 | intron variant | G/A;T | snv | 1 | |||
| rs2908972 | 1.000 | 0.040 | 17 | 11503942 | intron variant | T/A | snv | 0.39 | 1 | ||
| rs17428076 | 1.000 | 0.040 | 2 | 171987022 | intron variant | C/G | snv | 0.18 | 1 |