| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121908840 | 0.925 | 0.160 | 3 | 189867903 | missense variant | G/A | snv | 2 | |||
| rs886039442 | 0.925 | 0.160 | 3 | 189867906 | missense variant | G/A | snv | 2 | |||
| rs121908843 | 1.000 | 0.200 | 3 | 189890817 | missense variant | T/G | snv | 1 | |||
| rs121908842 | 1.000 | 0.200 | 3 | 189890795 | missense variant | A/T | snv | 1 | |||
| rs121908846 | 1.000 | 0.160 | 3 | 189890874 | missense variant | T/C;G | snv | 4.0E-06 | 1 | ||
| rs121908845 | 0.925 | 0.200 | 3 | 189889478 | missense variant | T/C | snv | 1 | |||
| rs121908847 | 0.925 | 0.240 | 3 | 189868641 | missense variant | A/G | snv | 1 | |||
| rs121908838 | 1.000 | 0.080 | 3 | 189864349 | missense variant | A/G | snv | 1 | |||
| rs121908835 | 0.882 | 0.240 | 3 | 189864379 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
| rs121908844 | 1.000 | 0.160 | 3 | 189868639 | missense variant | A/G | snv | 1 | |||
| rs121908849 | 0.925 | 0.240 | 3 | 189866712 | missense variant | G/A | snv | 1 | |||
| rs1205536026 | 1.000 | 0.160 | 3 | 189867902 | missense variant | C/T | snv | 1 | |||
| rs121908837 | 1.000 | 0.160 | 3 | 189868620 | missense variant | T/C | snv | 1 | |||
| rs121908839 | 0.925 | 0.160 | 3 | 189867905 | missense variant | C/T | snv | 1 | |||
| rs886041251 | 0.882 | 0.360 | 3 | 189868614 | missense variant | C/T | snv | 1 | |||
| rs121908841 | 1.000 | 0.160 | 3 | 189868615 | missense variant | G/A | snv | 1 | |||
| rs121908836 | 0.925 | 0.160 | 3 | 189864380 | missense variant | G/A | snv | 1.4E-05 | 1 |