Source: UNIPROT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs397516157 | 0.882 | 0.080 | 14 | 23424893 | missense variant | A/C;G;T | snv | 4.0E-06 | 1 | ||
| rs121913642 | 0.925 | 0.080 | 14 | 23427879 | missense variant | A/G | snv | 1 | |||
| rs397516269 | 0.882 | 0.080 | 14 | 23431426 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
| rs727503261 | 0.882 | 0.080 | 14 | 23425774 | missense variant | A/G;T | snv | 1 | |||
| rs267606911 | 0.882 | 0.080 | 14 | 23428587 | missense variant | C/A | snv | 8.0E-06 | 1 | ||
| rs121913624 | 0.851 | 0.080 | 14 | 23429278 | missense variant | C/A;G;T | snv | 1 | |||
| rs121913626 | 0.882 | 0.080 | 14 | 23427723 | missense variant | C/A;G;T | snv | 4.0E-06 | 1 | ||
| rs121913627 | 0.851 | 0.080 | 14 | 23427657 | missense variant | C/A;G;T | snv | 4.0E-06 | 1 | ||
| rs121913632 | 0.882 | 0.080 | 14 | 23425760 | missense variant | C/A;G;T | snv | 1 | |||
| rs121913647 | 0.925 | 0.160 | 14 | 23417173 | missense variant | C/A;G;T | snv | 1.6E-05 | 1 | ||
| rs2856897 | 0.925 | 0.080 | 14 | 23424875 | missense variant | C/A;G;T | snv | 4.0E-06; 1.2E-05 | 1 | ||
| rs3218716 | 0.716 | 0.280 | 14 | 23425316 | missense variant | C/A;G;T | snv | 4.0E-06; 2.4E-05 | 1 | ||
| rs36211715 | 0.851 | 0.080 | 14 | 23424839 | missense variant | C/A;G;T | snv | 4.0E-06 | 1 | ||
| rs397516101 | 0.882 | 0.080 | 14 | 23429004 | missense variant | C/A;G;T | snv | 1 | |||
| rs3218713 | 0.763 | 0.160 | 14 | 23431468 | missense variant | C/A;T | snv | 1 | |||
| rs397516202 | 0.882 | 0.080 | 14 | 23418244 | missense variant | C/A;T | snv | 7.0E-06 | 1 | ||
| rs397516260 | 0.882 | 0.080 | 14 | 23431789 | missense variant | C/A;T | snv | 1.6E-05 | 1 | ||
| rs730880759 | 0.925 | 0.080 | 14 | 23424068 | stop gained | C/A;T | snv | 4.0E-06 | 1 | ||
| rs121913628 | 0.763 | 0.160 | 14 | 23424059 | missense variant | C/G;T | snv | 1 | |||
| rs121913641 | 0.882 | 0.080 | 14 | 23425970 | missense variant | C/G;T | snv | 1 | |||
| rs397516088 | 0.882 | 0.080 | 14 | 23429850 | missense variant | C/G;T | snv | 1 | |||
| rs397516171 | 0.763 | 0.160 | 14 | 23424041 | missense variant | C/G;T | snv | 1 | |||
| rs727503260 | 0.851 | 0.080 | 14 | 23425403 | missense variant | C/G;T | snv | 1 | |||
| rs267606910 | 0.807 | 0.080 | 14 | 23431589 | missense variant | C/T | snv | 8.0E-06 | 2 | ||
| rs121913633 | 0.882 | 0.080 | 14 | 23431447 | missense variant | C/T | snv | 7.0E-06 | 1 |