| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs80356779 | 0.776 | 0.320 | 11 | 68780662 | missense variant | G/A | snv | 3.2E-05 | 5.6E-05 | 10 | |
| rs5030717 | 0.807 | 0.240 | 9 | 117711556 | intron variant | A/G | snv | 0.13 | 9 | ||
| rs1553155986 | 0.827 | 0.280 | 1 | 42929008 | missense variant | C/T | snv | 6 | |||
| rs1800028 | 0.925 | 0.040 | 19 | 48703560 | stop gained | C/G;T | snv | 5.6E-04 | 3 | ||
| rs10497394 | 0.925 | 0.040 | 2 | 173432931 | upstream gene variant | C/T | snv | 0.23 | 2 | ||
| rs766490137 | 0.925 | 0.040 | 3 | 52458801 | missense variant | T/C | snv | 4.0E-06 | 2 | ||
| rs16974263 | 1.000 | 0.040 | 19 | 40407632 | non coding transcript exon variant | C/T | snv | 0.28 | 1 | ||
| rs649057 | 1.000 | 0.040 | 9 | 99472041 | intron variant | C/A | snv | 8.2E-02 | 1 |