Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11074956 | 0.925 | 0.160 | 16 | 11243864 | downstream gene variant | G/T | snv | 0.34 | 2 | ||
rs12979659 | 0.925 | 0.160 | 19 | 6825021 | intron variant | T/C | snv | 0.36 | 0.28 | 2 | |
rs151719 | 0.925 | 0.160 | 6 | 32936123 | non coding transcript exon variant | C/T | snv | 0.72 | 2 | ||
rs17421624 | 0.925 | 0.160 | 6 | 32098400 | intron variant | T/C | snv | 0.25 | 2 | ||
rs2157051 | 0.925 | 0.160 | 6 | 32690847 | regulatory region variant | G/A | snv | 0.69 | 2 | ||
rs2524095 | 0.925 | 0.160 | 6 | 31298340 | intron variant | A/C | snv | 0.65 | 2 | ||
rs2546133 | 0.925 | 0.160 | 19 | 6799666 | intron variant | T/A;C | snv | 2 | |||
rs2617822 | 0.925 | 0.160 | 19 | 6801470 | intron variant | G/A;C | snv | 2 | |||
rs2621383 | 0.925 | 0.160 | 6 | 32791558 | intergenic variant | C/A | snv | 0.65 | 2 | ||
rs2621384 | 0.925 | 0.160 | 6 | 32791496 | intergenic variant | C/T | snv | 0.66 | 2 | ||
rs2849015 | 0.925 | 0.160 | 6 | 32231159 | intergenic variant | G/A | snv | 0.38 | 2 | ||
rs2857161 | 0.925 | 0.160 | 6 | 32791520 | intergenic variant | G/A | snv | 0.65 | 2 | ||
rs2894249 | 0.925 | 0.160 | 6 | 32358058 | intron variant | C/G;T | snv | 2 | |||
rs3129872 | 0.925 | 0.160 | 6 | 32439376 | upstream gene variant | A/T | snv | 0.24 | 2 | ||
rs3129877 | 0.925 | 0.160 | 6 | 32440820 | intron variant | G/A | snv | 0.26 | 2 | ||
rs3135342 | 0.925 | 0.160 | 6 | 32428838 | intergenic variant | G/T | snv | 0.24 | 2 | ||
rs3135377 | 0.925 | 0.160 | 6 | 32417622 | regulatory region variant | A/G | snv | 0.80 | 2 | ||
rs3135392 | 0.925 | 0.160 | 6 | 32441465 | intron variant | C/A | snv | 0.38 | 2 | ||
rs404890 | 0.925 | 0.160 | 6 | 32231090 | intergenic variant | C/A | snv | 0.35 | 2 | ||
rs486416 | 0.925 | 0.160 | 6 | 31888293 | intron variant | G/A | snv | 0.77 | 0.76 | 2 | |
rs6684865 | 0.925 | 0.160 | 1 | 2614790 | intron variant | G/A | snv | 0.40 | 2 | ||
rs682626 | 0.925 | 0.160 | 19 | 6774058 | intron variant | G/A;T | snv | 2 | |||
rs793108 | 0.925 | 0.160 | 10 | 31126177 | intron variant | C/T | snv | 0.40 | 2 | ||
rs9267873 | 0.925 | 0.160 | 6 | 32231575 | intergenic variant | C/G;T | snv | 2 | |||
rs9268429 | 0.925 | 0.160 | 6 | 32377275 | intron variant | A/G | snv | 0.24 | 2 |