| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104894369 | 0.807 | 0.080 | 12 | 110914287 | missense variant | C/A;T | snv | 10 | |||
| rs104894368 | 0.882 | 0.080 | 12 | 110919133 | stop gained | C/A;G;T | snv | 4.0E-06; 8.0E-06; 2.0E-05 | 4 | ||
| rs143139258 | 0.882 | 0.080 | 12 | 110913097 | missense variant | T/G | snv | 2.0E-04 | 2.9E-04 | 4 | |
| rs587782965 | 0.882 | 0.080 | 12 | 110914221 | missense variant | G/T | snv | 3 | |||
| rs199474815 | 0.925 | 0.080 | 12 | 110911081 | missense variant | T/A | snv | 2 | |||
| rs397516407 | 0.925 | 0.080 | 12 | 110911090 | missense variant | T/C;G | snv | 2 | |||
| rs104894363 | 1.000 | 0.080 | 12 | 110919160 | missense variant | C/T | snv | 3.7E-04 | 2.0E-04 | 1 | |
| rs104894370 | 1.000 | 0.080 | 12 | 110919145 | missense variant | A/G | snv | 1 | |||
| rs121913658 | 1.000 | 0.080 | 12 | 110913316 | missense variant | G/A;C | snv | 4.0E-06 | 1 | ||
| rs199474813 | 1.000 | 0.080 | 12 | 110911176 | splice acceptor variant | C/A;G;T | snv | 4.0E-06; 4.8E-05; 4.0E-06 | 1 | ||
| rs863225117 | 1.000 | 0.080 | 12 | 110915759 | missense variant | C/T | snv | 7.0E-06 | 1 |