| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs5443 | 0.532 | 0.760 | 12 | 6845711 | synonymous variant | C/T | snv | 0.36 | 0.44 | 106 | |
| rs222747 | 0.827 | 0.240 | 17 | 3589906 | missense variant | C/A;G;T | snv | 0.72; 4.5E-06 | 8 | ||
| rs211105 | 1.000 | 11 | 18033757 | intron variant | T/G | snv | 0.19 | 4 | |||
| rs1256318228 | 9 | 122386588 | synonymous variant | C/T | snv | 7.0E-06 | 1 | ||||
| rs4836884 | 9 | 122383715 | synonymous variant | C/G;T | snv | 4.0E-06; 2.8E-03 | 1 |