| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs876658511 | 1.000 | 0.040 | 9 | 21971147 | frameshift variant | TGGGCTCCGCGCCGTGGAGCAGCAGCAGCTCCGCCACT/- | delins | 1 | |||
| rs200429615 | 9 | 21971138 | missense variant | T/G | snv | 1 | |||||
| rs559848002 | 0.925 | 0.120 | 9 | 21971147 | missense variant | T/C;G | snv | 4.7E-06 | 1 | ||
| rs1390902532 | 1.000 | 0.040 | 9 | 21968766 | missense variant | T/C | snv | 7.4E-06 | 7.0E-06 | 2 | |
| rs1210653597 | 0.925 | 0.120 | 9 | 21968756 | missense variant | T/C | snv | 2 | |||
| rs1339638227 | 0.925 | 0.120 | 9 | 21971119 | missense variant | T/C | snv | 4.3E-06 | 2 | ||
| rs876658220 | 1.000 | 0.040 | 9 | 21971147 | frameshift variant | T/- | delins | 1 | |||
| rs387906410 | 0.882 | 0.080 | 9 | 21971019 | missense variant | GC/AG | mnv | 2 | |||
| rs1277299943 | 9 | 21974817 | missense variant | G/C | snv | 1.3E-05 | 1 | ||||
| rs104894104 | 0.790 | 0.160 | 9 | 21971019 | missense variant | G/A;T | snv | 3 | |||
| rs786204195 | 0.851 | 0.200 | 9 | 21974686 | missense variant | G/A;T | snv | 3 | |||
| rs1034265990 | 0.925 | 0.120 | 9 | 21971123 | missense variant | G/A;T | snv | 4.4E-06 | 2 | ||
| rs771138120 | 0.827 | 0.120 | 9 | 21971191 | missense variant | G/A;C;T | snv | 9.1E-06; 4.5E-06 | 13 | ||
| rs372266620 | 0.925 | 0.120 | 9 | 21971189 | missense variant | G/A;C;T | snv | 9.1E-05; 2.3E-05; 9.1E-06 | 1 | ||
| rs121913387 | 0.827 | 0.160 | 9 | 21971187 | stop gained | G/A;C | snv | 4.6E-06 | 4 | ||
| rs34886500 | 0.925 | 0.080 | 9 | 21971064 | missense variant | G/A;C | snv | 2 | |||
| rs11552823 | 1.000 | 0.040 | 9 | 21971117 | missense variant | G/A;C | snv | 4.3E-06 | 1 | ||
| rs1060504185 | 9 | 21971116 | missense variant | G/A;C | snv | 1 | |||||
| rs550846229 | 1.000 | 0.040 | 9 | 21974658 | missense variant | G/A;C | snv | 5.2E-05 | 1 | ||
| rs3088440 | 0.776 | 0.240 | 9 | 21968160 | 3 prime UTR variant | G/A | snv | 0.13 | 12 | ||
| rs755927351 | 1.000 | 0.040 | 9 | 21970968 | missense variant | G/A | snv | 4.1E-06 | 1 | ||
| rs4074785 | 1.000 | 0.080 | 9 | 21981584 | intron variant | G/A | snv | 0.12 | 1 | ||
| rs1453633223 | 0.807 | 0.080 | 9 | 21974503 | missense variant | C/T | snv | 4.0E-06 | 6 | ||
| rs1289280947 | 0.851 | 0.080 | 9 | 21974571 | missense variant | C/T | snv | 4.0E-06 | 5 | ||
| rs757066045 | 0.882 | 0.040 | 9 | 21974725 | missense variant | C/T | snv | 8.2E-06 | 4 |