| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1034395178 | 0.716 | 0.480 | 22 | 20996071 | stop gained | C/A;T | snv | 4.0E-06; 8.0E-06 | 33 | ||
| rs150419186 | 1.000 | 0.160 | 22 | 20989659 | stop gained | C/A;G;T | snv | 4.0E-06; 1.2E-05; 7.2E-05 | 2 | ||
| rs777243508 | 0.925 | 0.160 | 22 | 20993977 | stop gained | G/A | snv | 1.4E-04 | 1.8E-04 | 2 | |
| rs1249726034 | 1.000 | 0.160 | 22 | 20996679 | non coding transcript exon variant | C/A;G | snv | 4.0E-06; 4.0E-06; 4.0E-06 | 7.0E-06 | 1 | |
| rs1275511136 | 1.000 | 0.160 | 22 | 20997287 | missense variant | T/C;G | snv | 1 | |||
| rs1287917092 | 1.000 | 0.160 | 22 | 20989645 | missense variant | T/C | snv | 8.0E-06 | 1 | ||
| rs1327579827 | 1.000 | 0.160 | 22 | 20995995 | missense variant | C/A;G | snv | 1 | |||
| rs1374240053 | 1.000 | 0.160 | 22 | 20994629 | stop gained | G/A;C;T | snv | 4.0E-06 | 1 | ||
| rs1459786357 | 1.000 | 0.160 | 22 | 20982334 | 5 prime UTR variant | T/A;C | snv | 8.0E-06; 1.6E-05 | 1 | ||
| rs1569154492 | 1.000 | 0.160 | 22 | 20987544 | missense variant | C/G | snv | 1 | |||
| rs370638947 | 1.000 | 0.160 | 22 | 20995983 | missense variant | G/A;C;T | snv | 2.4E-05; 4.0E-06; 4.0E-06 | 1 | ||
| rs757502214 | 1.000 | 0.160 | 22 | 20988117 | missense variant | C/T | snv | 1.2E-05 | 2.8E-05 | 1 | |
| rs761685529 | 1.000 | 0.160 | 22 | 20995490 | splice region variant | C/T | snv | 4.1E-05 | 8.4E-05 | 1 | |
| rs762834512 | 1.000 | 0.160 | 22 | 20996740 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs770933647 | 1.000 | 0.160 | 22 | 20993712 | stop gained | G/A | snv | 7.0E-06 | 1 |