| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs886041761 | 0.925 | 0.200 | 1 | 110603902 | missense variant | C/T | snv | 6 | |||
| rs786205232 | 0.925 | 0.040 | 1 | 110603893 | missense variant | C/T | snv | 4.0E-06 | 5 | ||
| rs1064794738 | 1.000 | 0.040 | 1 | 110603588 | missense variant | C/T | snv | 1 | |||
| rs1553181280 | 1.000 | 0.040 | 1 | 110603663 | missense variant | T/C | snv | 1 | |||
| rs1553181282 | 1.000 | 0.040 | 1 | 110603665 | missense variant | G/A | snv | 1 | |||
| rs1553181301 | 1.000 | 0.040 | 1 | 110603770 | missense variant | C/T | snv | 1 | |||
| rs1553181323 | 1.000 | 0.040 | 1 | 110603824 | missense variant | G/A | snv | 1 | |||
| rs763353895 | 1.000 | 0.040 | 1 | 110604590 | stop gained | G/A | snv | 4.0E-06 | 1 | ||
| rs786205231 | 1.000 | 0.040 | 1 | 110603995 | missense variant | A/G | snv | 1 | |||
| rs876657389 | 1.000 | 0.040 | 1 | 110603569 | missense variant | G/A | snv | 1 | |||
| rs876657390 | 1.000 | 0.040 | 1 | 110603889 | missense variant | C/A | snv | 1 |