| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs119481075 | 0.882 | 0.240 | 9 | 96254906 | missense variant | C/T | snv | 8.8E-05 | 8.4E-05 | 4 | |
| rs119481077 | 0.882 | 0.240 | 9 | 96254907 | missense variant | G/A | snv | 3.2E-05 | 7.0E-06 | 3 | |
| rs28939085 | 0.882 | 0.240 | 9 | 96240885 | missense variant | G/A | snv | 2.0E-05 | 2.1E-05 | 3 | |
| rs747724352 | 0.925 | 0.240 | 9 | 96251474 | missense variant | C/T | snv | 2.0E-05 | 3 | ||
| rs119481076 | 0.925 | 0.240 | 9 | 96244393 | missense variant | G/A;T | snv | 2.0E-05; 8.0E-06 | 2 | ||
| rs144809928 | 0.925 | 0.240 | 9 | 96235548 | missense variant | G/A;C | snv | 3.2E-05; 4.0E-06 | 2 | ||
| rs201115371 | 0.925 | 0.240 | 9 | 96254864 | splice region variant | T/A | snv | 3.4E-04 | 3.7E-04 | 2 | |
| rs372027264 | 0.925 | 0.240 | 9 | 96244387 | stop gained | A/T | snv | 2.8E-05 | 3.5E-05 | 2 | |
| rs115063639 | 1.000 | 0.240 | 9 | 96244356 | missense variant | T/A;C | snv | 4.8E-05; 4.0E-06 | 1 | ||
| rs119481074 | 1.000 | 0.240 | 9 | 96240877 | missense variant | T/C | snv | 7.0E-06 | 1 | ||
| rs119481078 | 1.000 | 0.240 | 9 | 96298451 | missense variant | C/T | snv | 8.0E-06 | 1 | ||
| rs119481079 | 1.000 | 0.240 | 9 | 96251482 | missense variant | T/C | snv | 3.6E-05 | 3.5E-05 | 1 | |
| rs119481080 | 1.000 | 0.240 | 9 | 96240777 | missense variant | C/T | snv | 1 | |||
| rs747329682 | 1.000 | 0.240 | 9 | 96298423 | missense variant | G/A | snv | 1.2E-05 | 1 | ||
| rs780178733 | 1.000 | 0.240 | 9 | 96254924 | missense variant | T/C;G | snv | 1.6E-05; 1.6E-05 | 1 | ||
| rs142236065 | 1.000 | 0.240 | 9 | 96245352 | missense variant | G/A | snv | 1.6E-05 | 3.5E-05 | 1 | |
| rs767259718 | 1.000 | 0.240 | 9 | 96245424 | missense variant | T/C;G | snv | 4.0E-06; 8.0E-06 | 1 |