| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs762162799 | 0.776 | 0.120 | 3 | 48575437 | missense variant | C/G;T | snv | 8.6E-06; 4.3E-06; 3.0E-05 | 2 | ||
| rs147089666 | 1.000 | 0.080 | 3 | 48584508 | missense variant | G/A | snv | 8.0E-06; 4.0E-06 | 4.2E-05 | 1 | |
| rs121912856 | 0.732 | 0.120 | 3 | 48593538 | missense variant | T/C | snv | 3.2E-05 | 9.1E-05 | 1 | |
| rs121912855 | 0.851 | 0.200 | 3 | 48575218 | missense variant | G/A | snv | 2.0E-05 | 7.0E-06 | 1 | |
| rs121912849 | 1.000 | 0.080 | 3 | 48575236 | missense variant | G/A;C | snv | 8.0E-06; 4.0E-06 | 1 | ||
| rs760891216 | 1.000 | 0.080 | 3 | 48568819 | missense variant | C/T | snv | 2.1E-05 | 7.0E-06 | 1 | |
| rs755669902 | 1.000 | 0.080 | 3 | 48574549 | missense variant | C/T | snv | 1.2E-05 | 1.4E-05 | 1 | |
| rs121912853 | 1.000 | 0.080 | 3 | 48566719 | stop gained | C/A;T | snv | 1.2E-05 | 1 | ||
| rs121912851 | 1.000 | 0.080 | 3 | 48567736 | missense variant | C/T | snv | 1.4E-05 | 1 | ||
| rs1333259313 | 1.000 | 0.080 | 3 | 48566545 | missense variant | C/T | snv | 1.2E-05 | 2.1E-05 | 1 | |
| rs121912828 | 1.000 | 0.080 | 3 | 48566281 | missense variant | A/T | snv | 7.0E-06 | 1 | ||
| rs121912838 | 1.000 | 0.080 | 3 | 48575428 | missense variant | C/T | snv | 2.5E-05 | 2.1E-05 | 1 | |
| rs139318843 | 1.000 | 0.080 | 3 | 48568101 | missense variant | G/A | snv | 2.0E-05 | 4.9E-05 | 1 | |
| rs121912833 | 0.925 | 0.080 | 3 | 48584742 | missense variant | C/A;G;T | snv | 4.0E-06; 1.2E-05 | 1 | ||
| rs121912839 | 0.882 | 0.120 | 3 | 48572712 | missense variant | C/T | snv | 1 | |||
| rs766931219 | 1.000 | 0.080 | 3 | 48575445 | missense variant | C/G | snv | 4.2E-06 | 1 | ||
| rs121912831 | 1.000 | 0.080 | 3 | 48568098 | missense variant | C/A | snv | 1 | |||
| rs121912832 | 0.882 | 0.080 | 3 | 48575512 | missense variant | C/T | snv | 1 | |||
| rs121912846 | 1.000 | 0.080 | 3 | 48575409 | missense variant | C/T | snv | 1 | |||
| rs1553854678 | 1.000 | 0.080 | 3 | 48575355 | missense variant | C/T | snv | 1 | |||
| rs121912844 | 0.925 | 0.080 | 3 | 48575419 | missense variant | C/T | snv | 4.2E-06 | 1 | ||
| rs121912842 | 1.000 | 0.080 | 3 | 48575502 | missense variant | C/T | snv | 1 | |||
| rs121912836 | 0.882 | 0.080 | 3 | 48575392 | missense variant | C/A;T | snv | 1 | |||
| rs121912829 | 1.000 | 0.080 | 3 | 48575401 | missense variant | C/T | snv | 1 | |||
| rs387906605 | 0.925 | 0.080 | 3 | 48582512 | missense variant | C/T | snv | 1 |