| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121908740 | 0.882 | 0.160 | 20 | 44623054 | missense variant | G/A | snv | 1.3E-04 | 7.0E-06 | 3 | |
| rs121908722 | 0.925 | 0.160 | 20 | 44625580 | missense variant | C/A;G;T | snv | 2 | |||
| rs121908718 | 0.925 | 0.160 | 20 | 44621103 | missense variant | G/A;T | snv | 8.0E-06; 2.8E-05 | 2 | ||
| rs1194494050 | 1.000 | 0.160 | 20 | 44620435 | non coding transcript exon variant | C/T | snv | 4.0E-06 | 1 | ||
| rs121908729 | 1.000 | 0.160 | 20 | 44622911 | missense variant | G/A | snv | 1 | |||
| rs387906268 | 1.000 | 0.160 | 20 | 44619862 | intron variant | A/T | snv | 1 |