Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs145013566 | 2 | 218297998 | intron variant | -/C | ins | 5 | |||||
rs34001204 | 2 | 218314933 | intron variant | A/- | del | 0.44 | 1 | ||||
rs2382817 | 0.925 | 0.040 | 2 | 218286495 | 5 prime UTR variant | A/C | snv | 0.61 | 3 | ||
rs2382818 | 2 | 218291184 | intron variant | A/T | snv | 0.36 | 1 | ||||
rs4674280 | 2 | 218276735 | intron variant | C/G | snv | 0.50 | 2 | ||||
rs1870125 | 2 | 218323178 | 5 prime UTR variant | C/G;T | snv | 2 | |||||
rs13020391 | 0.790 | 0.080 | 2 | 218319713 | intron variant | C/T | snv | 0.32 | 9 | ||
rs2271543 | 2 | 218277768 | intron variant | C/T | snv | 0.35 | 1 | ||||
rs4791 | 2 | 218274217 | 3 prime UTR variant | C/T | snv | 0.44 | 1 | ||||
rs992157 | 0.790 | 0.080 | 2 | 218290058 | 5 prime UTR variant | G/A | snv | 0.46 | 9 | ||
rs2292553 | 2 | 218282080 | missense variant | G/A | snv | 0.55 | 0.43 | 2 | |||
rs1877712 | 2 | 218303709 | intron variant | G/A | snv | 0.43 | 2 | ||||
rs897877 | 2 | 218328032 | intron variant | G/A | snv | 0.49 | 1 | ||||
rs1017698 | 2 | 218305802 | intron variant | G/A;C | snv | 1 | |||||
rs1870123 | 2 | 218322975 | intron variant | G/A;C | snv | 1 | |||||
rs3731861 | 0.776 | 0.080 | 2 | 218326533 | intron variant | T/C | snv | 0.32 | 10 | ||
rs10716631 | 2 | 218273447 | intron variant | T/G | snv | 1 |