Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11285463 | 6 | 104944130 | intron variant | TT/-;T;TTT | delins | 1 | |||||
rs113772882 | 7 | 1602560 | intergenic variant | G/A;T | snv | 1 | |||||
rs114285994 | 16 | 19924441 | intergenic variant | G/A;C | snv | 1 | |||||
rs11534296 | 9 | 80667487 | intergenic variant | G/A;C | snv | 1 | |||||
rs11578152 | 1 | 102111465 | intergenic variant | A/G;T | snv | 1 | |||||
rs11715566 | 3 | 117843589 | intron variant | C/A;T | snv | 1 | |||||
rs11767400 | 7 | 122520688 | intron variant | C/A;T | snv | 1 | |||||
rs11893331 | 2 | 56350271 | intron variant | A/C;G;T | snv | 1 | |||||
rs12472911 | 2 | 141470940 | intron variant | C/A;T | snv | 1 | |||||
rs12603280 | 17 | 6131434 | intergenic variant | G/A;C | snv | 1 | |||||
rs12879819 | 14 | 77958440 | intergenic variant | C/A;G;T | snv | 1 | |||||
rs12926791 | 16 | 69815643 | intron variant | C/A;G;T | snv | 1 | |||||
rs13053505 | 22 | 38849613 | intergenic variant | G/A;C;T | snv | 1 | |||||
rs1398217 | 18 | 47225867 | intron variant | G/C;T | snv | 1 | |||||
rs1400974 | 2 | 198773966 | upstream gene variant | G/A;C | snv | 1 | |||||
rs1456522 | 2 | 198904459 | intron variant | A/G;T | snv | 1 | |||||
rs17817628 | 17 | 55097366 | intron variant | A/C;G | snv | 1 | |||||
rs17817995 | 17 | 55335233 | intergenic variant | G/A;C | snv | 1 | |||||
rs17854357 | 11 | 65834089 | splice region variant | G/C;T | snv | 0.12; 5.8E-05 | 1 | ||||
rs1860826 | 7 | 2072871 | intron variant | G/A;T | snv | 1 | |||||
rs1888072 | 9 | 89591072 | intron variant | T/C;G | snv | 1 | |||||
rs1915146 | 10 | 125157645 | intron variant | A/C;G;T | snv | 1 | |||||
rs1973284 | 1 | 243693379 | intron variant | A/G;T | snv | 1 | |||||
rs201205097 | 2 | 613044 | intergenic variant | -/AC | delins | 1 | |||||
rs2063730 | 11 | 78337478 | intron variant | A/C;G | snv | 1 |