| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12813018 | 12 | 73160218 | intron variant | T/A | snv | 0.28 | 1 | ||||
| rs12826112 | 12 | 73162120 | intron variant | T/C | snv | 0.28 | 1 | ||||
| rs1976729 | 12 | 73159309 | non coding transcript exon variant | G/A;C;T | snv | 1 | |||||
| rs1976730 | 12 | 73159402 | non coding transcript exon variant | A/G | snv | 0.28 | 1 | ||||
| rs2176205 | 12 | 73159438 | non coding transcript exon variant | C/T | snv | 0.28 | 1 | ||||
| rs7299264 | 12 | 73159557 | intron variant | A/C;T | snv | 1 | |||||
| rs7302852 | 12 | 73163388 | intron variant | C/A | snv | 0.28 | 1 | ||||
| rs7960698 | 12 | 73158334 | upstream gene variant | C/G;T | snv | 1 | |||||
| rs9614326 | 22 | 44103463 | non coding transcript exon variant | A/C | snv | 3.6E-02 | 1 | ||||
| rs2244144 | 1 | 156214807 | intron variant | G/A | 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 | ||||
| rs2758600 | 1 | 156225414 | intron variant | C/T | snv | 0.30 | 1 | ||||
| rs2758607 | 1 | 156232968 | intron variant | G/A;T | snv | 1 | |||||
| rs2758608 | 1 | 156233069 | intron variant | A/G;T | snv | 1 | |||||
| rs2853643 | 1 | 156215040 | intron variant | G/A | snv | 0.30 | 1 | ||||
| rs2853646 | 1 | 156219835 | intron variant | C/T | snv | 0.30 | 1 | ||||
| rs6427307 | 1 | 156220292 | intron variant | A/G;T | snv | 1 | |||||
| rs7534434 | 1 | 156216824 | intron variant | A/G;T | snv | 1 | |||||
| rs887953 | 1 | 156221358 | intron variant | T/C | snv | 0.36 | 1 | ||||
| rs1060604 | 1 | 156214477 | intron variant | T/C | snv | 0.30 | 1 | ||||
| rs1137703 | 1 | 156214667 | intron variant | T/A;C | snv | 1 | |||||
| rs2251636 | 1 | 156233018 | intron variant | G/C | snv | 0.41 | 1 | ||||
| rs2251847 | 1 | 156234256 | intron variant | G/A | snv | 0.38 | 1 | ||||
| rs2540173 | 1 | 156218423 | intron variant | A/G | snv | 0.43 | 1 |