| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4977574 | 0.695 | 0.520 | 9 | 22098575 | intron variant | A/G;T | snv | 26 | |||
| rs28939702 | 0.851 | 0.320 | 16 | 16154899 | missense variant | G/A;T | snv | 8.2E-05 | 13 | ||
| rs63751001 | 0.790 | 0.240 | 16 | 16159555 | missense variant | C/T | snv | 2.8E-05 | 13 | ||
| rs72650700 | 0.827 | 0.240 | 16 | 16190247 | stop gained | G/A;T | snv | 4.4E-05; 4.0E-06 | 12 | ||
| rs60791294 | 0.882 | 0.280 | 16 | 16163086 | missense variant | C/G;T | snv | 7.6E-05 | 11 | ||
| rs63750759 | 0.851 | 0.280 | 16 | 16154974 | missense variant | G/A;T | snv | 1.9E-04; 5.4E-06 | 11 | ||
| rs66492417 | 0.882 | 0.240 | 16 | 16178909 | stop gained | G/T | snv | 10 | |||
| rs63749796 | 0.925 | 0.200 | 16 | 16159505 | missense variant | C/G | snv | 9 | |||
| rs63750410 | 0.882 | 0.240 | 16 | 16155007 | missense variant | C/G;T | snv | 6.0E-06; 1.2E-05 | 9 | ||
| rs63750622 | 0.925 | 0.200 | 16 | 16154898 | missense variant | C/A;G;T | snv | 4.1E-06; 4.1E-06; 1.6E-05 | 9 | ||
| rs72664223 | 1.000 | 0.160 | 16 | 16221763 | frameshift variant | T/- | del | 4.1E-06 | 9 | ||
| rs1555513085 | 0.925 | 0.200 | 16 | 16182486 | frameshift variant | TCTC/- | delins | 8 | |||
| rs761433545 | 0.925 | 0.200 | 16 | 16187192 | missense variant | C/A;G;T | snv | 2.0E-05 | 8 | ||
| rs78678589 | 0.925 | 0.160 | 16 | 16203457 | missense variant | G/C;T | snv | 1.6E-05 | 8 | ||
| rs63751111 | 1.000 | 0.160 | 16 | 16154873 | missense variant | C/G;T | snv | 8.1E-06 | 7 | ||
| rs72653783 | 1.000 | 0.160 | 16 | 16182566 | missense variant | T/G | snv | 4.0E-06 | 7 | ||
| rs1555512158 | 0.925 | 0.200 | 16 | 16177554 | missense variant | C/G | snv | 6 | |||
| rs1555514467 | 1.000 | 0.160 | 16 | 16188897 | frameshift variant | AG/- | delins | 6 | |||
| rs63750428 | 0.925 | 0.200 | 16 | 16154767 | missense variant | G/A;T | snv | 4.9E-05 | 6 | ||
| rs72653769 | 1.000 | 0.160 | 16 | 16190315 | missense variant | A/T | snv | 8.0E-06 | 6 | ||
| rs72664203 | 1.000 | 0.160 | 16 | 16219948 | splice acceptor variant | C/G | snv | 6 | |||
| rs72664239 | 0.925 | 0.200 | 16 | 16150646 | frameshift variant | C/- | delins | 6 | |||
| rs749125777 | 1.000 | 0.160 | 16 | 16173287 | missense variant | G/A;C | snv | 4.0E-06; 8.0E-06 | 6 | ||
| rs769437554 | 0.925 | 0.200 | 16 | 16165784 | inframe deletion | AAG/- | delins | 1.2E-05 | 6 | ||
| rs776513864 | 0.925 | 0.200 | 16 | 16178920 | missense variant | G/A;C | snv | 1.2E-05; 4.0E-06 | 6 |