| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10131751 | 1.000 | 0.040 | 14 | 28212010 | intergenic variant | C/A | snv | 9.2E-02 | 1 | ||
| rs10167914 | 1.000 | 0.040 | 2 | 112805784 | TF binding site variant | A/G | snv | 0.31 | 1 | ||
| rs10508881 | 1.000 | 0.040 | 10 | 44046117 | regulatory region variant | A/G | snv | 0.50 | 1 | ||
| rs113850637 | 1.000 | 0.040 | 3 | 104131556 | intergenic variant | C/T | snv | 0.14 | 1 | ||
| rs1432089 | 1.000 | 0.040 | 4 | 170869637 | intergenic variant | C/T | snv | 0.37 | 1 | ||
| rs1448792 | 1.000 | 0.040 | 9 | 22641634 | upstream gene variant | A/G | snv | 0.71 | 1 | ||
| rs1537377 | 1.000 | 0.040 | 9 | 22169701 | regulatory region variant | T/C | snv | 0.44 | 1 | ||
| rs1903068 | 1.000 | 0.040 | 4 | 55142310 | intergenic variant | A/G | snv | 0.25 | 1 | ||
| rs1995051 | 1.000 | 0.040 | 7 | 45885442 | upstream gene variant | A/G | snv | 0.70 | 1 | ||
| rs2738113 | 1.000 | 0.040 | 8 | 6971563 | upstream gene variant | G/A;T | snv | 1 | |||
| rs4654783 | 1.000 | 0.040 | 1 | 22113027 | downstream gene variant | T/C | snv | 0.70 | 1 | ||
| rs60966186 | 1.000 | 0.040 | 8 | 6973682 | upstream gene variant | A/G | snv | 1 | |||
| rs6542095 | 1.000 | 0.040 | 2 | 112771606 | downstream gene variant | C/A;T | snv | 1 | |||
| rs6757804 | 1.000 | 0.040 | 2 | 150779318 | regulatory region variant | C/T | snv | 0.58 | 1 | ||
| rs71415016 | 1.000 | 0.040 | 14 | 95977621 | intergenic variant | T/C | snv | 6.1E-02 | 1 | ||
| rs7781172 | 1.000 | 0.040 | 7 | 49030398 | intergenic variant | G/A;T | snv | 1 | |||
| rs811 | 1.000 | 0.040 | 12 | 90382160 | intergenic variant | C/A;T | snv | 1 | |||
| rs855965 | 1.000 | 0.040 | 10 | 117684248 | intergenic variant | G/A | snv | 0.40 | 1 | ||
| rs9356708 | 1.000 | 0.040 | 6 | 19728772 | intron variant | T/A;G | snv | 1 | |||
| rs3820445 | 1.000 | 0.040 | 1 | 48758912 | missense variant | G/A;T | snv | 1 | |||
| rs74781061 | 1.000 | 0.040 | 15 | 74595855 | 3 prime UTR variant | A/G | snv | 0.31 | 1 | ||
| rs777161444 | 1.000 | 0.040 | 1 | 150817123 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs4837864 | 1.000 | 0.040 | 9 | 116782154 | intron variant | T/C | snv | 0.84 | 1 | ||
| rs498679 | 1.000 | 0.040 | 6 | 106122200 | intron variant | T/A;C | snv | 1 | |||
| rs144824657 | 1.000 | 0.040 | 19 | 577782 | missense variant | G/A;T | snv | 9.7E-05; 5.5E-03 | 1 |