| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4656461 | 0.827 | 0.040 | 1 | 165717968 | TF binding site variant | G/A | snv | 0.85 | 7 | ||
| rs1015213 | 0.851 | 0.040 | 8 | 51974981 | intron variant | C/T | snv | 0.14 | 6 | ||
| rs10483727 | 0.851 | 0.040 | 14 | 60606157 | upstream gene variant | T/C | snv | 0.45 | 4 | ||
| rs7081455 | 0.851 | 0.040 | 10 | 20349956 | upstream gene variant | G/A;T | snv | 4 | |||
| rs17752199 | 0.925 | 0.040 | 6 | 51542050 | upstream gene variant | A/C;G;T | snv | 3 | |||
| rs3858145 | 0.882 | 0.040 | 10 | 68252081 | regulatory region variant | A/G | snv | 0.33 | 3 | ||
| rs547984 | 0.882 | 0.040 | 1 | 237933586 | intergenic variant | A/C | snv | 0.60 | 3 | ||
| rs6478746 | 0.925 | 0.040 | 9 | 126605119 | intron variant | G/A | snv | 0.72 | 3 | ||
| rs9853115 | 0.925 | 0.040 | 3 | 186413811 | intergenic variant | T/A;G | snv | 0.51 | 3 | ||
| rs10281637 | 1.000 | 0.040 | 7 | 116511284 | downstream gene variant | T/C | snv | 0.28 | 2 | ||
| rs2022945 | 1.000 | 0.040 | 8 | 107238911 | intergenic variant | A/G | snv | 0.87 | 2 | ||
| rs2188836 | 1.000 | 0.040 | 7 | 117995328 | downstream gene variant | C/T | snv | 0.41 | 2 | ||
| rs1013278 | 1.000 | 0.040 | 7 | 117963766 | regulatory region variant | G/A;C | snv | 1 | |||
| rs10152898 | 1.000 | 0.040 | 15 | 73962780 | intergenic variant | G/A;T | snv | 1 | |||
| rs190298731 | 1.000 | 0.040 | 6 | 148738155 | intergenic variant | A/C;T | snv | 1 | |||
| rs2024211 | 1.000 | 0.040 | 7 | 116512971 | downstream gene variant | A/C | snv | 0.27 | 1 | ||
| rs2935057 | 1.000 | 0.040 | 6 | 170139691 | intron variant | A/G;T | snv | 1 | |||
| rs3116139 | 1.000 | 0.040 | 19 | 51375780 | upstream gene variant | C/A;T | snv | 1 | |||
| rs504022 | 1.000 | 0.040 | 21 | 43311258 | regulatory region variant | T/G | snv | 0.91 | 1 | ||
| rs56233426 | 1.000 | 0.040 | 3 | 186411027 | intergenic variant | A/G | snv | 0.50 | 1 | ||
| rs61861119 | 1.000 | 0.040 | 10 | 93182666 | intergenic variant | A/G | snv | 0.45 | 1 | ||
| rs8141433 | 1.000 | 0.040 | 22 | 19866483 | intergenic variant | A/G;T | snv | 1 | |||
| rs7034696 | 1.000 | 0.040 | 9 | 18804132 | intron variant | C/T | snv | 0.27 | 1 | ||
| rs1042713 | 0.576 | 0.800 | 5 | 148826877 | missense variant | G/A | snv | 0.42 | 0.43 | 63 | |
| rs28500712 | 1.000 | 0.040 | 4 | 7894486 | intron variant | A/C;G | snv | 2 |