| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs200198778 | 0.827 | 0.160 | 14 | 77278764 | missense variant | T/C | snv | 5.6E-05 | 9.8E-05 | 5 | |
| rs961440747 | 0.882 | 0.120 | 14 | 77320433 | splice donor variant | C/A;G | snv | 1.4E-05 | 3 | ||
| rs1185491348 | 0.882 | 0.120 | 14 | 77285042 | splice acceptor variant | CT/- | del | 7.0E-06 | 3 | ||
| rs147871747 | 0.882 | 0.120 | 14 | 77302843 | stop gained | G/A;C;T | snv | 1.4E-04; 1.2E-05; 4.0E-06 | 3 | ||
| rs1555351894 | 0.882 | 0.120 | 14 | 77280051 | frameshift variant | GT/- | delins | 3 | |||
| rs1555352706 | 0.882 | 0.120 | 14 | 77286782 | frameshift variant | -/G | delins | 3 | |||
| rs368817785 | 0.882 | 0.120 | 14 | 77285548 | stop gained | G/A | snv | 1.2E-05 | 7.0E-06 | 3 | |
| rs775932206 | 0.882 | 0.120 | 14 | 77298737 | stop gained | G/A | snv | 1.2E-05 | 3 | ||
| rs886044256 | 0.882 | 0.120 | 14 | 77298773 | splice acceptor variant | T/C;G | snv | 7.0E-06 | 3 | ||
| rs267606967 | 1.000 | 14 | 77277386 | missense variant | C/G | snv | 1 | ||||
| rs267606971 | 1.000 | 14 | 77302940 | missense variant | G/A | snv | 4.0E-06 | 1 | |||
| rs587780422 | 1.000 | 14 | 77298684 | splice region variant | C/T | snv | 2.0E-05 | 1 | |||
| rs587780423 | 1.000 | 14 | 77299497 | missense variant | T/C | snv | 4.0E-06; 1.2E-05 | 2.1E-05 | 1 | ||
| rs727502855 | 1.000 | 14 | 77286815 | missense variant | G/A;C | snv | 2.4E-05; 1.2E-05 | 1 |