| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2842873 | 1 | 156234862 | intron variant | C/G;T | snv | 1 | |||||
| rs7312029 | 12 | 73155046 | upstream gene variant | C/G;T | snv | 1 | |||||
| rs7960698 | 12 | 73158334 | upstream gene variant | C/G;T | snv | 1 | |||||
| rs368869806 | 0.614 | 0.480 | 9 | 95485875 | splice acceptor variant | C/T | snv | 4.0E-06 | 7.0E-06 | 97 | |
| rs10161441 | 12 | 73136489 | intron variant | C/T | snv | 0.27 | 1 | ||||
| rs10879568 | 12 | 73156497 | upstream gene variant | C/T | snv | 0.28 | 1 | ||||
| rs10879572 | 12 | 73157791 | upstream gene variant | C/T | snv | 0.28 | 1 | ||||
| rs11179580 | 12 | 73192799 | intron variant | C/T | snv | 0.27 | 1 | ||||
| rs2176205 | 12 | 73159438 | non coding transcript exon variant | C/T | snv | 0.28 | 1 | ||||
| rs2736609 | 1 | 156232849 | intron variant | C/T | snv | 0.34 | 1 | ||||
| rs2758600 | 1 | 156225414 | intron variant | C/T | snv | 0.30 | 1 | ||||
| rs2853646 | 1 | 156219835 | intron variant | C/T | snv | 0.30 | 1 | ||||
| rs2984613 | 1 | 156227589 | intron variant | C/T | snv | 0.32 | 1 | ||||
| rs7311904 | 12 | 73154963 | upstream gene variant | C/T | snv | 0.28 | 1 | ||||
| rs11655160 | 17 | 10989753 | intergenic variant | G/A | snv | 0.19 | 1 | ||||
| rs2244144 | 1 | 156214807 | intron variant | G/A | snv | 0.30 | 1 | ||||
| rs2251847 | 1 | 156234256 | intron variant | G/A | snv | 0.38 | 1 | ||||
| rs2758598 | 1 | 156224548 | intron variant | G/A | snv | 0.30 | 1 | ||||
| rs2758609 | 1 | 156233077 | intron variant | G/A | snv | 0.34 | 1 | ||||
| rs2842865 | 1 | 156189741 | upstream gene variant | G/A | snv | 0.42 | 1 | ||||
| rs2853643 | 1 | 156215040 | intron variant | G/A | snv | 0.30 | 1 | ||||
| rs10879567 | 12 | 73156312 | upstream gene variant | G/A;C | snv | 1 | |||||
| rs2842864 | 1 | 156189426 | upstream gene variant | G/A;C | snv | 1 | |||||
| rs11179569 | 12 | 73153274 | intergenic variant | G/A;C;T | snv | 1 | |||||
| rs1976729 | 12 | 73159309 | non coding transcript exon variant | G/A;C;T | snv | 1 |