| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4263839 | 0.807 | 0.160 | 9 | 114804160 | intron variant | A/G | snv | 0.75 | 7 | ||
| rs148292941 | 1 | 161171095 | stop gained | T/C;G | snv | 8.0E-06 | 6.3E-05 | 4 | |||
| rs1672753 | 0.882 | 0.240 | 3 | 3179746 | upstream gene variant | C/T | snv | 0.71 | 4 | ||
| rs121913371 | 1.000 | 0.040 | 7 | 140781678 | missense variant | G/A;T | snv | 4.0E-06; 8.0E-06 | 3 | ||
| rs6768972 | 1.000 | 0.160 | 3 | 3180101 | upstream gene variant | A/C;G | snv | 2 | |||
| rs6090453 | 1.000 | 0.040 | 20 | 62724010 | intron variant | C/A;G;T | snv | 2 | |||
| rs1800832 | 12 | 85874401 | 5 prime UTR variant | A/G | snv | 8.2E-02 | 7.6E-02 | 1 |