Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1131691014 | 0.439 | 0.800 | 17 | 7676154 | frameshift variant | -/C | ins | 214 | |||
rs11935941 | 1.000 | 0.040 | 4 | 148731326 | intron variant | A/C | snv | 0.31 | 2 | ||
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
rs4149570 | 0.752 | 0.360 | 12 | 6342424 | upstream gene variant | A/C;G;T | snv | 11 | |||
rs7041 | 0.576 | 0.800 | 4 | 71752617 | missense variant | A/C;T | snv | 0.52; 4.0E-06 | 64 | ||
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 121 | |
rs5498 | 0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 | 99 | |
rs731236 | 0.542 | 0.760 | 12 | 47844974 | synonymous variant | A/G | snv | 0.33 | 0.34 | 81 | |
rs1800469 | 0.547 | 0.760 | 19 | 41354391 | intron variant | A/G | snv | 0.69 | 78 | ||
rs744166 | 0.689 | 0.560 | 17 | 42362183 | intron variant | A/G | snv | 0.48 | 22 | ||
rs3850641 | 0.716 | 0.400 | 1 | 173206693 | intron variant | A/G | snv | 0.14 | 17 | ||
rs10774625 | 0.763 | 0.320 | 12 | 111472415 | intron variant | A/G | snv | 0.66 | 13 | ||
rs179247 | 0.882 | 0.160 | 14 | 80966202 | intron variant | A/G | snv | 0.40 | 5 | ||
rs30461 | 0.827 | 0.120 | 19 | 39298475 | missense variant | A/G | snv | 0.13 | 0.25 | 5 | |
rs17759659 | 0.851 | 0.120 | 18 | 63291411 | intron variant | A/G | snv | 0.31 | 4 | ||
rs6543116 | 0.882 | 0.120 | 2 | 102311266 | upstream gene variant | A/G | snv | 0.76 | 3 | ||
rs7171171 | 0.925 | 0.120 | 15 | 38614840 | intergenic variant | A/G | snv | 0.24 | 3 | ||
rs7629750 | 0.882 | 0.040 | 3 | 119455829 | intron variant | A/G | snv | 0.45 | 3 | ||
rs853326 | 0.882 | 0.120 | 8 | 132897729 | missense variant | A/G | snv | 0.58 | 0.60 | 3 | |
rs1269486 | 0.925 | 0.120 | 10 | 8054236 | intron variant | A/G | snv | 0.77 | 2 | ||
rs2227478 | 0.925 | 0.040 | 12 | 68254842 | upstream gene variant | A/G | snv | 0.37 | 2 | ||
rs4411444 | 0.925 | 0.120 | 14 | 80978764 | intron variant | A/G | snv | 0.43 | 2 | ||
rs756763 | 1.000 | 0.040 | 17 | 51671952 | intron variant | A/G | snv | 0.48 | 2 | ||
rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 223 | ||
rs231775 | 0.504 | 0.720 | 2 | 203867991 | missense variant | A/G;T | snv | 0.42; 4.0E-06 | 115 |