| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1553574522 | 1.000 | 0.040 | 2 | 165331362 | missense variant | T/C | snv | 1 | |||
| rs200138205 | 1.000 | 0.040 | 2 | 165365200 | missense variant | G/A;C | snv | 1.7E-04; 3.2E-05 | 1 | ||
| rs121918799 | 0.752 | 0.120 | 2 | 166015636 | missense variant | G/C | snv | 1.7E-03 | 1.6E-03 | 14 | |
| rs121918817 | 0.882 | 0.040 | 2 | 166045080 | missense variant | C/T | snv | 1.7E-03 | 1.5E-03 | 3 | |
| rs180922748 | 1.000 | 0.040 | 2 | 166233432 | missense variant | G/C | snv | 1.2E-03 | 1.7E-03 | 1 | |
| rs199692186 | 1.000 | 0.040 | 2 | 166272748 | missense variant | T/C | snv | 6.3E-04 | 5.5E-04 | 1 | |
| rs765818027 | 1.000 | 0.040 | 2 | 166293358 | missense variant | C/T | snv | 4.6E-05 | 2.8E-05 | 1 | |
| rs147896487 | 1.000 | 0.040 | 8 | 18084767 | missense variant | C/G | snv | 1.3E-03 | 1.5E-03 | 1 | |
| rs202162520 | 1.000 | 0.040 | 16 | 2496317 | missense variant | C/A;T | snv | 4.0E-06; 1.9E-03 | 1 | ||
| rs765965968 | 0.882 | 0.080 | 16 | 2498333 | missense variant | G/A;T | snv | 1.3E-05; 4.2E-06 | 5 | ||
| rs1383795440 | 1.000 | 0.040 | 22 | 31754865 | 5 prime UTR variant | G/C | snv | 7.0E-06 | 1 | ||
| rs768456731 | 0.925 | 0.040 | 22 | 31765049 | missense variant | G/A;T | snv | 1.6E-05 | 2 | ||
| rs187334123 | 1.000 | 0.040 | 22 | 31797646 | missense variant | G/A;T | snv | 2.2E-03; 1.6E-05 | 1 | ||
| rs1555897392 | 1.000 | 0.040 | 22 | 31838822 | protein altering variant | -/AGA | ins | 1 | |||
| rs886039266 | 0.925 | 0.040 | 22 | 31870703 | frameshift variant | A/- | del | 2 | |||
| rs138450474 | 1.000 | 0.040 | 19 | 35039140 | missense variant | G/A;C | snv | 2.0E-05 | 1 | ||
| rs202020647 | 1.000 | 0.040 | 1 | 37540752 | missense variant | G/A | snv | 1.8E-04 | 1.3E-04 | 1 | |
| rs1553155982 | 1.000 | 0.040 | 1 | 42928996 | missense variant | T/A | snv | 1 | |||
| rs1553138299 | 1.000 | 0.040 | 1 | 43403254 | missense variant | C/G | snv | 1 | |||
| rs747241860 | 1.000 | 0.040 | 1 | 43428297 | missense variant | C/T | snv | 8.4E-05 | 1.4E-05 | 1 | |
| rs752473314 | 1.000 | 0.040 | 1 | 43428455 | missense variant | C/T | snv | 1.6E-05 | 1.4E-05 | 1 | |
| rs780805483 | 1.000 | 0.040 | 1 | 43435233 | missense variant | G/A;T | snv | 4.0E-06; 1.2E-05 | 1 | ||
| rs1306918506 | 1.000 | 0.040 | 1 | 43439950 | missense variant | A/T | snv | 8.0E-06 | 1 | ||
| rs748723710 | 1.000 | 0.040 | 1 | 43442281 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs1553154643 | 1.000 | 0.040 | 1 | 43443774 | missense variant | C/T | snv | 1 |