| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104894484 | 1.000 | 0.120 | 15 | 68211793 | missense variant | C/T | snv | 1 | |||
| rs104894486 | 1.000 | 0.120 | 15 | 68209639 | stop gained | G/A;C | snv | 1 | |||
| rs1194940137 | 1.000 | 0.120 | 15 | 68208187 | missense variant | G/T | snv | 4.0E-06 | 1 | ||
| rs121908079 | 1.000 | 0.120 | 15 | 68211289 | inframe deletion | ATA/- | delins | 1 | |||
| rs1381427322 | 1.000 | 0.120 | 15 | 68229502 | missense variant | C/T | snv | 1.2E-05 | 1 | ||
| rs150363441 | 1.000 | 0.120 | 15 | 68208301 | missense variant | C/A;G;T | snv | 2.4E-05 | 1 | ||
| rs154774639 | 1.000 | 0.120 | 15 | 68208186 | frameshift variant | G/- | delins | 1.4E-05 | 1 | ||
| rs1555438212 | 1.000 | 0.120 | 15 | 68208239 | stop gained | C/T | snv | 1 | |||
| rs1555438229 | 1.000 | 0.120 | 15 | 68208288 | frameshift variant | -/AG | delins | 1 | |||
| rs1555438234 | 1.000 | 0.120 | 15 | 68208306 | frameshift variant | TGTCC/- | delins | 1 | |||
| rs1555438255 | 1.000 | 0.120 | 15 | 68208354 | missense variant | A/G | snv | 1 | |||
| rs1555438411 | 1.000 | 0.120 | 15 | 68209637 | stop gained | C/T | snv | 1 | |||
| rs1555438443 | 1.000 | 0.120 | 15 | 68209759 | stop gained | C/T | snv | 1 | |||
| rs1555438614 | 1.000 | 0.120 | 15 | 68211262 | splice donor variant | C/A | snv | 1 | |||
| rs1555440188 | 1.000 | 0.120 | 15 | 68229500 | splice donor variant | A/C | snv | 1 | |||
| rs1555440206 | 1.000 | 0.120 | 15 | 68229584 | start lost | T/C | snv | 1 | |||
| rs1567095153 | 1.000 | 0.120 | 15 | 68209749 | frameshift variant | -/G | delins | 1 | |||
| rs1567096598 | 1.000 | 0.120 | 15 | 68214337 | missense variant | A/T | snv | 1 | |||
| rs374681194 | 1.000 | 0.120 | 15 | 68208321 | missense variant | C/A;T | snv | 2.0E-04 | 1 | ||
| rs553192210 | 1.000 | 0.120 | 15 | 68214177 | non coding transcript exon variant | C/A;G | snv | 2.8E-05 | 1 | ||
| rs746753722 | 1.000 | 0.120 | 15 | 68208397 | missense variant | C/T | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs747229909 | 1.000 | 0.120 | 15 | 68211716 | missense variant | G/A;C | snv | 5.6E-05 | 1 | ||
| rs758921701 | 1.000 | 0.120 | 15 | 68208180 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs762902907 | 1.000 | 0.120 | 15 | 68211306 | frameshift variant | -/A | delins | 4.0E-06 | 7.0E-06 | 1 | |
| rs763944821 | 1.000 | 0.120 | 15 | 68229536 | missense variant | C/T | snv | 8.2E-04 | 9.8E-05 | 1 |