| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1935157 | 1 | 221143916 | intergenic variant | C/A;G | snv | 1 | |||||
| rs201395463 | 1 | 7942040 | intron variant | GGA/-;GGAGGA | delins | 6.0E-03 | 1 | ||||
| rs2061705 | 1 | 102976258 | intron variant | A/G;T | snv | 1 | |||||
| rs2076586 | 1 | 111730404 | intron variant | C/T | snv | 0.19 | 1 | ||||
| rs213010 | 1 | 21312674 | intron variant | A/G | snv | 0.39 | 1 | ||||
| rs213624 | 1 | 25874673 | upstream gene variant | G/A | snv | 0.51 | 1 | ||||
| rs2275560 | 1 | 164560429 | non coding transcript exon variant | G/A | snv | 0.37 | 1 | ||||
| rs2279469 | 1 | 164771168 | non coding transcript exon variant | G/C | snv | 0.52 | 1 | ||||
| rs2335077 | 1 | 107030943 | intergenic variant | A/G | snv | 0.32 | 1 | ||||
| rs2605110 | 1 | 219481050 | intergenic variant | C/T | snv | 0.61 | 1 | ||||
| rs2613505 | 1 | 72369727 | intron variant | C/T | snv | 0.85 | 1 | ||||
| rs2742690 | 1 | 3070704 | intron variant | C/A;T | snv | 0.13 | 1 | ||||
| rs2765539 | 1 | 119006795 | TF binding site variant | C/G;T | snv | 1 | |||||
| rs2791550 | 1 | 219482027 | intergenic variant | T/G | snv | 0.61 | 1 | ||||
| rs2791644 | 1 | 11100617 | intron variant | C/G;T | snv | 1 | |||||
| rs2798603 | 1 | 154819793 | intron variant | G/A;C | snv | 1 | |||||
| rs2800847 | 1 | 221953542 | intron variant | G/A | snv | 0.26 | 1 | ||||
| rs2820464 | 1 | 219519878 | intergenic variant | G/A;C | snv | 1 | |||||
| rs2821391 | 1 | 200067662 | intron variant | A/G | snv | 0.36 | 1 | ||||
| rs2903995 | 1 | 22945011 | intergenic variant | T/A | snv | 0.37 | 1 | ||||
| rs2993481 | 1 | 3056869 | downstream gene variant | A/T | snv | 0.24 | 1 | ||||
| rs3119837 | 1 | 170382972 | intergenic variant | C/A;T | snv | 1 | |||||
| rs313732 | 1 | 85792920 | intron variant | A/G | snv | 0.33 | 1 | ||||
| rs313741 | 1 | 85807768 | intron variant | A/C;T | snv | 1 | |||||
| rs36043408 | 1 | 203542364 | intergenic variant | G/A;T | snv | 1 |