Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 116 | |
| rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 81 | |
| rs79105258 | 12 | 111280427 | intron variant | C/A;T | snv | 24 | |||||
| rs1169288 | 0.776 | 0.160 | 12 | 120978847 | missense variant | A/C;T | snv | 0.35 | 21 | ||
| rs17145750 | 0.925 | 0.120 | 7 | 73612048 | intron variant | C/A;T | snv | 9 | |||
| rs11066453 | 1.000 | 0.080 | 12 | 112927816 | intron variant | A/G | snv | 3.8E-03 | 4 |