Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 121 | |
rs763361 | 0.689 | 0.520 | 18 | 69864406 | missense variant | T/A;C | snv | 4.0E-06; 0.52 | 21 | ||
rs2076530 | 0.724 | 0.640 | 6 | 32396039 | missense variant | T/C | snv | 0.42 | 0.40 | 17 | |
rs5844572 | 0.752 | 0.360 | 22 | 23893562 | intron variant | -/ATTC | delins | 11 | |||
rs9277554 | 0.790 | 0.520 | 6 | 33087761 | 3 prime UTR variant | C/T | snv | 0.38 | 7 | ||
rs42041 | 0.882 | 0.280 | 7 | 92617430 | intron variant | C/G | snv | 0.21 | 3 | ||
rs6922466 | 0.882 | 0.240 | 6 | 138123793 | regulatory region variant | A/G | snv | 0.21 | 3 | ||
rs7503953 | 0.882 | 0.320 | 17 | 6238357 | intergenic variant | A/C | snv | 0.81 | 3 | ||
rs9277341 | 0.882 | 0.280 | 6 | 33071848 | intron variant | T/A;C | snv | 3 | |||
rs730881997 | 0.925 | 0.200 | 17 | 7675999 | missense variant | A/C;T | snv | 8.0E-06 | 4 | ||
rs10548957 | 0.925 | 0.200 | 6 | 33195861 | non coding transcript exon variant | AG/- | delins | 2 | |||
rs118099717 | 0.925 | 0.200 | 4 | 84604268 | missense variant | G/C | snv | 1.2E-03 | 9.1E-04 | 2 | |
rs151269264 | 0.925 | 0.200 | 22 | 50738307 | synonymous variant | G/A;C | snv | 1.6E-05; 6.0E-05 | 2 | ||
rs1949829 | 0.925 | 0.200 | 7 | 51470190 | upstream gene variant | C/T | snv | 0.12 | 2 | ||
rs26595 | 0.925 | 0.200 | 5 | 116423793 | intergenic variant | G/A;T | snv | 2 | |||
rs3117242 | 0.925 | 0.200 | 6 | 33102116 | upstream gene variant | A/G | snv | 0.34 | 2 | ||
rs595018 | 0.925 | 0.200 | 11 | 60824803 | upstream gene variant | T/A;C | snv | 2 | |||
rs6531 | 0.925 | 0.200 | 6 | 33195674 | synonymous variant | G/A | snv | 0.77 | 0.77 | 2 |