Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 262 | |
rs855791 | 0.701 | 0.400 | 22 | 37066896 | missense variant | A/G;T | snv | 0.57; 4.0E-06 | 38 | ||
rs3811647 | 0.807 | 0.120 | 3 | 133765185 | intron variant | G/A | snv | 0.31 | 15 | ||
rs174577 | 1.000 | 0.080 | 11 | 61837342 | intron variant | C/A | snv | 0.38 | 13 | ||
rs8177240 | 3 | 133758857 | intron variant | T/C;G | snv | 0.29 | 5 | ||||
rs744653 | 2 | 189514024 | regulatory region variant | C/T | snv | 0.84 | 4 | ||||
rs9990333 | 3 | 196100334 | intergenic variant | C/T | snv | 0.42 | 4 | ||||
rs8177179 | 0.925 | 0.080 | 3 | 133744613 | intron variant | G/A | snv | 0.58 | 4 | ||
rs6486121 | 11 | 13334223 | intron variant | C/T | snv | 0.53 | 3 | ||||
rs4921915 | 8 | 18414956 | intergenic variant | G/A | snv | 0.71 | 2 |