| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs760545501 | 2 | 224359374 | regulatory region variant | C/T | snv | 1.2E-04 | 1 | ||||
| rs761310536 | 1.000 | 0.120 | 21 | 46121115 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 2 | |
| rs769783985 | 0.925 | 0.120 | 2 | 227052395 | missense variant | C/G;T | snv | 1.2E-05 | 2.1E-05 | 3 | |
| rs779593707 | 1 | 16049884 | stop gained | -/AATA | delins | 1.2E-05 | 7.0E-06 | 2 | |||
| rs797044813 | 1.000 | 0.120 | X | 50090490 | stop gained | C/T | snv | 2 | |||
| rs9644778 | 8 | 7052132 | downstream gene variant | A/C | snv | 0.34 | 1 |