| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121434578 | 1.000 | 0.080 | 16 | 8768248 | missense variant | G/A | snv | 5 | |||
| rs724159990 | 1.000 | 0.080 | 16 | 8768220 | missense variant | C/T | snv | 5 | |||
| rs724159992 | 1.000 | 0.080 | 16 | 8750498 | missense variant | G/A | snv | 1.4E-05 | 5 | ||
| rs724159991 | 1.000 | 0.080 | 16 | 8781360 | missense variant | T/C | snv | 5 | |||
| rs1330995774 | 1.000 | 0.080 | 16 | 8776350 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs1555492932 | 1.000 | 0.080 | 16 | 8772778 | splice acceptor variant | A/G | snv | 1 | |||
| rs1567300736 | 1.000 | 0.080 | 16 | 8746099 | splice donor variant | G/A | snv | 1 | |||
| rs1567310537 | 1.000 | 0.080 | 16 | 8764744 | missense variant | C/T | snv | 1 | |||
| rs1567312671 | 1.000 | 0.080 | 16 | 8768227 | missense variant | T/G | snv | 1 | |||
| rs1057523345 | 1.000 | 0.080 | 16 | 8781321 | missense variant | G/A | snv | 1 | |||
| rs1555494322 | 1.000 | 0.080 | 16 | 8781387 | missense variant | T/C | snv | 1 | |||
| rs781555217 | 1.000 | 0.080 | 16 | 8781320 | stop gained | G/A;C;T | snv | 4.0E-06; 4.0E-06 | 1 |