Source: BEFREE
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1137101 | 0.554 | 0.760 | 1 | 65592830 | missense variant | A/G | snv | 0.51 | 0.50 | 77 | |
| rs1137100 | 0.627 | 0.640 | 1 | 65570758 | missense variant | A/G | snv | 0.30 | 0.25 | 39 | |
| rs1805094 | 0.716 | 0.440 | 1 | 65610269 | missense variant | G/C;T | snv | 0.16; 4.0E-06 | 16 | ||
| rs1256046734 | 0.763 | 0.280 | 1 | 65621409 | missense variant | A/G | snv | 7.0E-06 | 12 | ||
| rs1805096 | 0.827 | 0.200 | 1 | 65636574 | synonymous variant | G/A | snv | 0.46 | 0.43 | 5 | |
| rs8179183 | 1.000 | 0.080 | 1 | 65610269 | missense variant | G/C;T | snv | 3 | |||
| rs757574299 | 1.000 | 0.080 | 1 | 65570511 | missense variant | C/G | snv | 1.6E-05 | 1.4E-05 | 2 | |
| rs11804091 | 1.000 | 0.080 | 1 | 65438196 | intron variant | A/G | snv | 0.15 | 1 | ||
| rs1329162134 | 1.000 | 0.080 | 1 | 65605061 | missense variant | T/C | snv | 7.0E-06 | 1 | ||
| rs2025804 | 1.000 | 0.080 | 1 | 65480438 | intron variant | G/A | snv | 0.69 | 1 | ||
| rs373154589 | 1.000 | 0.080 | 1 | 65616036 | missense variant | G/C | snv | 8.0E-06 | 1.4E-05 | 1 |