| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1271401320 | 1.000 | 0.120 | 9 | 21440749 | missense variant | A/G | snv | 3 | |||
| rs104893825 | 1.000 | 0.120 | 3 | 10149819 | missense variant | G/T | snv | 2 | |||
| rs1131690964 | 1.000 | 0.120 | 3 | 10142124 | frameshift variant | G/- | delins | 2 | |||
| rs193922608 | 1.000 | 0.120 | 3 | 10142089 | missense variant | C/A;T | snv | 4.3E-06; 4.3E-06 | 2 | ||
| rs193922609 | 1.000 | 0.120 | 3 | 10142167 | missense variant | G/A;C | snv | 2 | |||
| rs398123481 | 1.000 | 0.120 | 3 | 10142103 | missense variant | C/G;T | snv | 2 | |||
| rs5030802 | 1.000 | 0.120 | 3 | 10142055 | stop gained | G/A;T | snv | 4.4E-06 | 2 | ||
| rs5030829 | 1.000 | 0.120 | 3 | 10142127 | stop gained | G/A;T | snv | 4.5E-06 | 2 | ||
| rs587780077 | 1.000 | 0.120 | 3 | 10146618 | missense variant | G/A;C;T | snv | 2 | |||
| rs730882031 | 1.000 | 0.120 | 3 | 10142039 | frameshift variant | C/- | del | 2 | |||
| rs765978945 | 1.000 | 0.120 | 3 | 10142180 | missense variant | C/G;T | snv | 4.5E-06 | 2 | ||
| rs786202787 | 1.000 | 0.120 | 3 | 10142085 | missense variant | A/C;G | snv | 2 | |||
| rs864622109 | 1.000 | 0.120 | 3 | 10149878 | stop gained | C/G;T | snv | 2 | |||
| rs869025615 | 1.000 | 0.120 | 3 | 10142009 | frameshift variant | G/-;GG | delins | 2 | |||
| rs869025618 | 1.000 | 0.120 | 3 | 10142061 | missense variant | T/C | snv | 2 | |||
| rs869025631 | 1.000 | 0.120 | 3 | 10142179 | missense variant | G/A;T | snv | 2 | |||
| rs1064793878 | 1.000 | 0.120 | 3 | 10149874 | missense variant | T/C | snv | 1 | |||
| rs1347416980 | 1.000 | 0.120 | 3 | 10146568 | missense variant | A/C;G | snv | 4.0E-06 | 1 | ||
| rs1352275281 | 1.000 | 0.120 | 3 | 10149815 | missense variant | G/C;T | snv | 8.0E-06 | 1 | ||
| rs1368606697 | 1.000 | 0.120 | 1 | 161356763 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs143985153 | 1.000 | 0.120 | 3 | 10142116 | missense variant | A/C;G;T | snv | 1 | |||
| rs1553619402 | 1.000 | 0.120 | 3 | 10142035 | frameshift variant | -/G | delins | 1 | |||
| rs1553619415 | 1.000 | 0.120 | 3 | 10142052 | frameshift variant | -/G | delins | 1 | |||
| rs1553619440 | 1.000 | 0.120 | 3 | 10142125 | missense variant | G/A;T | snv | 1 | |||
| rs1553619461 | 1.000 | 0.120 | 3 | 10142160 | missense variant | A/C | snv | 1 |