| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs77375493 | 0.458 | 0.760 | 9 | 5073770 | missense variant | G/A;T | snv | 3.5E-04 | 187 | ||
| rs61752717 | 0.583 | 0.840 | 16 | 3243407 | missense variant | T/A;C | snv | 2.8E-04 | 72 | ||
| rs121913530 | 0.583 | 0.640 | 12 | 25245351 | missense variant | C/A;G;T | snv | 63 | |||
| rs121913682 | 0.605 | 0.400 | 4 | 54733167 | missense variant | A/G;T | snv | 52 | |||
| rs121913237 | 0.611 | 0.560 | 1 | 114716126 | missense variant | C/A;G;T | snv | 8.0E-06 | 50 | ||
| rs121913507 | 0.614 | 0.400 | 4 | 54733155 | missense variant | A/T | snv | 49 | |||
| rs121913506 | 0.677 | 0.320 | 4 | 54733154 | missense variant | G/A;C;T | snv | 24 | |||
| rs371769427 | 0.683 | 0.400 | 21 | 43104346 | missense variant | G/A;T | snv | 8.0E-06 | 24 | ||
| rs1057519710 | 0.695 | 0.280 | 4 | 54733166 | missense variant | G/C;T | snv | 22 | |||
| rs147001633 | 0.776 | 0.240 | 2 | 25234373 | missense variant | C/A;G;T | snv | 4.0E-06; 4.0E-06; 2.2E-04 | 15 | ||
| rs559063155 | 0.732 | 0.280 | 2 | 197402110 | stop gained | T/A;C;G | snv | 9.0E-05 | 14 | ||
| rs371246226 | 0.827 | 0.160 | 21 | 43094667 | missense variant | T/C;G | snv | 2.4E-05; 2.4E-05 | 8 | ||
| rs377577594 | 0.827 | 0.240 | 2 | 25234374 | missense variant | G/A;C;T | snv | 1.2E-04; 8.0E-06 | 7 | ||
| rs1464681682 | 0.882 | 0.160 | 21 | 6486334 | missense variant | T/C;G | snv | 6 | |||
| rs587779821 | 1.000 | 0.080 | 11 | 108259059 | missense variant | A/G;T | snv | 2 | |||
| rs569067880 | 0.925 | 0.080 | 4 | 105234864 | missense variant | G/A;C | snv | 4.0E-06; 4.0E-06 | 2 | ||
| rs761064473 | 1.000 | 0.080 | 2 | 25240717 | missense variant | C/G;T | snv | 1.2E-05 | 1 | ||
| rs1554481435 | 1.000 | 0.080 | 7 | 148809351 | missense variant | C/T | snv | 1 | |||
| rs114619974 | 1.000 | 0.080 | 4 | 105234376 | missense variant | G/A | snv | 5.2E-04 | 2.2E-03 | 1 | |
| rs1283441077 | 1.000 | 0.080 | 4 | 105276331 | missense variant | C/T | snv | 6.4E-06 | 1 | ||
| rs1316795626 | 1.000 | 0.080 | 4 | 105276287 | missense variant | G/A | snv | 6.4E-06 | 1 | ||
| rs532738858 | 1.000 | 0.080 | 4 | 105236763 | missense variant | C/T | snv | 1.2E-05 | 2.1E-05 | 1 | |
| rs116519313 | 1.000 | 0.080 | 4 | 105276128 | missense variant | T/C;G | snv | 1.3E-05 | 1 | ||
| rs1406914931 | 1.000 | 0.080 | 4 | 105276431 | missense variant | G/T | snv | 1 | |||
| rs376570662 | 1.000 | 0.080 | 4 | 105235321 | missense variant | C/T | snv | 1.2E-04 | 1.7E-04 | 1 |