| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs770085172 | 1.000 | 0.160 | 1 | 230710315 | missense variant | T/C | snv | 7.0E-06 | 1 | ||
| rs758748662 | 1.000 | 0.160 | 7 | 55155911 | missense variant | G/A | snv | 4.0E-06 | 1.4E-05 | 1 | |
| rs771366736 | 1.000 | 0.160 | 7 | 55143380 | missense variant | A/G | snv | 8.0E-06 | 1.4E-05 | 1 | |
| rs771929085 | 1.000 | 0.160 | 7 | 55155941 | missense variant | G/A | snv | 1.2E-05 | 1 | ||
| rs1340806384 | 1.000 | 0.160 | 19 | 45364442 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs140522180 | 1.000 | 0.160 | 19 | 45353112 | missense variant | C/A;T | snv | 2.0E-05; 1.9E-04 | 1 | ||
| rs746795177 | 1.000 | 0.160 | 19 | 45364121 | splice acceptor variant | T/C | snv | 1.3E-05 | 1.4E-05 | 1 | |
| rs752510317 | 1.000 | 0.160 | 19 | 45352556 | missense variant | G/A | snv | 1.2E-05 | 1 | ||
| rs753641926 | 1.000 | 0.160 | 19 | 45353113 | missense variant | G/A;T | snv | 4.4E-05; 4.0E-06 | 1 | ||
| rs758439420 | 1.000 | 0.160 | 19 | 45352351 | missense variant | C/A;T | snv | 8.0E-06; 1.6E-05 | 1 | ||
| rs767747355 | 1.000 | 0.160 | 19 | 45364838 | frameshift variant | GAGT/- | delins | 1.2E-05 | 1 | ||
| rs771824813 | 1.000 | 0.160 | 19 | 45353109 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs772572683 | 1.000 | 0.160 | 19 | 45355676 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs200919197 | 1.000 | 0.160 | 16 | 85481 | missense variant | C/G;T | snv | 1.2E-05; 9.6E-05 | 1 | ||
| rs1312839452 | 1.000 | 0.160 | 19 | 54982237 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
| rs1194327405 | 1.000 | 0.160 | X | 71377774 | missense variant | G/A | snv | 1.1E-05 | 1 | ||
| rs1225118391 | 0.925 | 0.200 | 1 | 230710637 | missense variant | T/C | snv | 4.0E-06 | 2 | ||
| rs369137693 | 0.925 | 0.200 | 2 | 69193414 | missense variant | C/T | snv | 2.8E-05 | 1.4E-05 | 2 | |
| rs747908253 | 0.925 | 0.200 | 2 | 69182599 | missense variant | G/A | snv | 1.6E-05 | 2 | ||
| rs148298598 | 0.925 | 0.200 | 14 | 20457111 | missense variant | G/A | snv | 2.3E-04 | 2.1E-04 | 2 | |
| rs80357091 | 1.000 | 0.160 | 17 | 43104910 | missense variant | A/C;G | snv | 8.0E-06 | 2 | ||
| rs1180868926 | 0.925 | 0.200 | 3 | 9757095 | missense variant | A/G | snv | 4.0E-06 | 2 | ||
| rs761032372 | 0.925 | 0.200 | 3 | 9759215 | missense variant | C/A;T | snv | 8.0E-06 | 2 | ||
| rs121913025 | 0.925 | 0.240 | 19 | 45357295 | missense variant | A/G | snv | 2 | |||
| rs139002770 | 0.925 | 0.200 | 19 | 45352772 | missense variant | C/T | snv | 8.0E-06 | 2 |