| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1057519803 | 0.925 | 0.080 | 12 | 56088138 | missense variant | G/A | snv | 4 | |||
| rs121913247 | 0.882 | 0.200 | 7 | 116783359 | missense variant | T/C | snv | 3 | |||
| rs876660572 | 1.000 | 0.080 | 5 | 112815549 | missense variant | A/G | snv | 7.0E-06 | 2 | ||
| rs758204762 | 0.925 | 0.080 | 17 | 39712330 | missense variant | G/A;C | snv | 4.0E-06; 1.6E-05 | 2 | ||
| rs756090401 | 1.000 | 0.080 | 5 | 112835036 | missense variant | A/G | snv | 8.0E-06 | 1.4E-05 | 1 | |
| rs1452020002 | 1.000 | 0.080 | 2 | 211947467 | missense variant | G/C;T | snv | 1 | |||
| rs773197447 | 1.000 | 0.080 | 4 | 1807159 | missense variant | G/A;C | snv | 3.2E-05; 2.3E-05 | 1 | ||
| rs1345316856 | 1.000 | 0.080 | 8 | 27810979 | missense variant | A/C | snv | 4.0E-06 | 1 | ||
| rs4872077 | 1.000 | 0.080 | 8 | 23200675 | intron variant | T/A;C | snv | 0.29 | 1 |