| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2244144 | 1 | 156214807 | intron variant | G/A | snv | 0.30 | 1 | ||||
| rs2540175 | 1 | 156214956 | intron variant | T/C | snv | 0.43 | 1 | ||||
| rs2853643 | 1 | 156215040 | intron variant | G/A | snv | 0.30 | 1 | ||||
| rs7534434 | 1 | 156216824 | intron variant | A/G;T | snv | 1 | |||||
| rs2540173 | 1 | 156218423 | intron variant | A/G | snv | 0.43 | 1 | ||||
| rs2853646 | 1 | 156219835 | intron variant | C/T | snv | 0.30 | 1 | ||||
| rs6427307 | 1 | 156220292 | intron variant | A/G;T | snv | 1 | |||||
| rs887953 | 1 | 156221358 | intron variant | T/C | snv | 0.36 | 1 | ||||
| rs2758598 | 1 | 156224548 | intron variant | G/A | snv | 0.30 | 1 | ||||
| rs2758600 | 1 | 156225414 | intron variant | C/T | snv | 0.30 | 1 | ||||
| rs2248074 | 1 | 156226097 | intron variant | C/A;T | snv | 1 | |||||
| rs2736613 | 1 | 156226225 | intron variant | T/C | snv | 0.35 | 1 | ||||
| rs2984613 | 1 | 156227589 | intron variant | C/T | snv | 0.32 | 1 | ||||
| rs3001789 | 1 | 156227823 | intron variant | T/G | snv | 0.37 | 1 | ||||
| rs2758603 | 1 | 156229203 | intron variant | T/C | snv | 0.37 | 2 | ||||
| rs2758605 | 1 | 156230654 | intron variant | G/C | snv | 0.37 | 1 | ||||
| rs2842870 | 1 | 156230880 | intron variant | T/A;C | snv | 2 | |||||
| rs1052053 | 1.000 | 0.080 | 1 | 156232382 | missense variant | A/C;G | snv | 1.0E-03; 0.38 | 3 | ||
| rs2736609 | 1 | 156232849 | intron variant | C/T | snv | 0.34 | 1 | ||||
| rs2758607 | 1 | 156232968 | intron variant | G/A;T | snv | 1 | |||||
| rs2251636 | 1 | 156233018 | intron variant | G/C | snv | 0.41 | 1 | ||||
| rs2758608 | 1 | 156233069 | intron variant | A/G;T | snv | 1 | |||||
| rs2758609 | 1 | 156233077 | intron variant | G/A | snv | 0.34 | 1 | ||||
| rs2251847 | 1 | 156234256 | intron variant | G/A | snv | 0.38 | 1 | ||||
| rs2842873 | 1 | 156234862 | intron variant | C/G;T | snv | 1 |