| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1553630457 | 0.882 | 0.240 | 3 | 30674231 | missense variant | T/C | snv | 8 | |||
| rs104893810 | 0.790 | 0.360 | 3 | 30691477 | missense variant | C/T | snv | 7 | |||
| rs104893819 | 0.827 | 0.240 | 3 | 30688470 | stop gained | C/G;T | snv | 5 | |||
| rs104893811 | 0.851 | 0.160 | 3 | 30674228 | missense variant | C/T | snv | 4 | |||
| rs104893815 | 0.851 | 0.240 | 3 | 30691478 | missense variant | G/A | snv | 4 | |||
| rs863223852 | 0.882 | 0.120 | 3 | 30688476 | stop gained | C/A;T | snv | 4.0E-06 | 4 | ||
| rs886039551 | 0.882 | 0.120 | 3 | 30674186 | missense variant | G/A | snv | 4 | |||
| rs104893809 | 0.882 | 0.120 | 3 | 30691504 | missense variant | C/T | snv | 3 | |||
| rs104893816 | 0.882 | 0.120 | 3 | 30674229 | missense variant | G/A;T | snv | 4.0E-06 | 3 | ||
| rs727504292 | 0.882 | 0.120 | 3 | 30672250 | missense variant | G/A;C | snv | 1.6E-05 | 3 | ||
| rs727504421 | 0.882 | 0.160 | 3 | 30691465 | missense variant | G/A;T | snv | 3 | |||
| rs104893807 | 0.925 | 0.120 | 3 | 30674196 | missense variant | C/G;T | snv | 2 | |||
| rs193922664 | 0.925 | 0.120 | 3 | 30691435 | missense variant | T/C | snv | 2 | |||
| rs104893812 | 1.000 | 0.120 | 3 | 30672189 | missense variant | T/A;G | snv | 1 | |||
| rs104893813 | 1.000 | 0.120 | 3 | 30672246 | missense variant | G/A;C;T | snv | 8.2E-06; 8.2E-06 | 1 | ||
| rs104893814 | 1.000 | 0.120 | 3 | 30672252 | missense variant | G/T | snv | 1 | |||
| rs104893817 | 1.000 | 0.120 | 3 | 30674123 | missense variant | A/C;G | snv | 1 | |||
| rs104893818 | 1.000 | 0.120 | 3 | 30674130 | missense variant | C/T | snv | 1 | |||
| rs121918715 | 1.000 | 0.120 | 3 | 30688511 | splice region variant | G/A | snv | 1 | |||
| rs1553630274 | 1.000 | 0.120 | 3 | 30672313 | missense variant | A/G | snv | 1 | |||
| rs28934568 | 1.000 | 0.120 | 3 | 30672106 | missense variant | T/C | snv | 1 | |||
| rs587776770 | 1.000 | 0.120 | 3 | 30688382 | splice acceptor variant | A/G | snv | 1 | |||
| rs761231369 | 1.000 | 0.120 | 3 | 30671923 | missense variant | A/T | snv | 8.0E-06 | 1.4E-05 | 1 | |
| rs780542125 | 1.000 | 0.120 | 3 | 30671752 | missense variant | G/A | snv | 5.2E-05 | 2.8E-05 | 1 | |
| rs863223853 | 1.000 | 0.120 | 3 | 30691421 | missense variant | G/T | snv | 1 |