| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs397507476 | 0.882 | 0.200 | 7 | 140778011 | missense variant | T/A;G | snv | 4 | |||
| rs397507481 | 0.882 | 0.240 | 7 | 140754206 | missense variant | G/C;T | snv | 4 | |||
| rs180177034 | 0.882 | 0.200 | 7 | 140801536 | missense variant | C/G | snv | 3 | |||
| rs397507469 | 0.882 | 0.200 | 7 | 140801503 | missense variant | G/T | snv | 3 | |||
| rs397516893 | 0.925 | 0.160 | 7 | 140778048 | missense variant | A/C | snv | 3 | |||
| rs794729219 | 0.882 | 0.240 | 7 | 140753352 | missense variant | A/G | snv | 3 | |||
| rs121913337 | 0.925 | 0.200 | 7 | 140753353 | missense variant | A/C;T | snv | 2 | |||
| rs121913349 | 0.925 | 0.200 | 7 | 140781618 | missense variant | C/G;T | snv | 2 | |||
| rs180177036 | 0.925 | 0.200 | 7 | 140778053 | missense variant | C/A;G | snv | 2 | |||
| rs397507475 | 0.925 | 0.200 | 7 | 140778054 | missense variant | A/G | snv | 2 | |||
| rs397516903 | 0.925 | 0.200 | 7 | 140801533 | missense variant | A/C;G | snv | 2 | |||
| rs397516904 | 0.925 | 0.200 | 7 | 140801487 | missense variant | T/C;G | snv | 2 | |||
| rs727502904 | 0.925 | 0.200 | 7 | 140734763 | missense variant | G/A;T | snv | 2 | |||
| rs727504375 | 0.925 | 0.200 | 7 | 140778059 | missense variant | T/G | snv | 2 | |||
| rs180177037 | 1.000 | 0.160 | 7 | 140778013 | missense variant | T/C | snv | 1 | |||
| rs397507465 | 1.000 | 0.160 | 7 | 140801542 | missense variant | T/G | snv | 1 | |||
| rs397507470 | 1.000 | 0.160 | 7 | 140801488 | missense variant | G/T | snv | 1 | |||
| rs397507473 | 1.000 | 0.160 | 7 | 140781605 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
| rs397507474 | 1.000 | 0.160 | 7 | 140778061 | missense variant | T/C;G | snv | 4.0E-06 | 1 | ||
| rs397507479 | 1.000 | 0.160 | 7 | 140777011 | missense variant | C/T | snv | 1 | |||
| rs397507480 | 1.000 | 0.160 | 7 | 140754233 | missense variant | A/C | snv | 1 | |||
| rs397507486 | 1.000 | 0.160 | 7 | 140739813 | missense variant | T/C | snv | 1 | |||
| rs397516892 | 1.000 | 0.160 | 7 | 140778066 | missense variant | G/T | snv | 1 | |||
| rs397516894 | 1.000 | 0.160 | 7 | 140754208 | missense variant | G/A;C | snv | 1 | |||
| rs869025606 | 1.000 | 0.160 | 7 | 140781609 | missense variant | A/C | snv | 1 |