| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2723341 | 0.807 | 0.160 | 15 | 71811481 | splice acceptor variant | A/C | snv | 5.3E-04 | 5.1E-04 | 8 | |
| rs28937873 | 0.807 | 0.160 | 15 | 71813573 | missense variant | G/A | snv | 4.0E-04 | 3.1E-04 | 7 | |
| rs121912631 | 0.851 | 0.080 | 15 | 71811530 | missense variant | G/A;T | snv | 4 | |||
| rs1555454566 | 0.882 | 0.160 | 15 | 71811553 | inframe deletion | ACGGCTGCA/- | delins | 3 | |||
| rs1567160967 | 1.000 | 0.080 | 15 | 71814051 | frameshift variant | TGCAG/- | del | 1 | |||
| rs730882149 | 1.000 | 0.080 | 15 | 71811507 | frameshift variant | GC/AGTGTGCCTCCAGTGCCTCGCTCCA | delins | 1 |