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 | 34 | |
rs653178 | 0.672 | 0.600 | 12 | 111569952 | intron variant | C/T | snv | 0.67 | 23 | ||
rs2155219 | 0.732 | 0.280 | 11 | 76588150 | upstream gene variant | G/T | snv | 0.52 | 10 | ||
rs9275524 | 0.807 | 0.160 | 6 | 32707332 | upstream gene variant | T/C | snv | 0.58 | 6 | ||
rs694739 | 0.763 | 0.320 | 11 | 64329761 | upstream gene variant | A/G | snv | 0.28 | 6 | ||
rs9275572 | 0.724 | 0.360 | 6 | 32711222 | upstream gene variant | A/G;T | snv | 4 | |||
rs1701704 | 0.851 | 0.200 | 12 | 56018703 | intron variant | T/G | snv | 0.25 | 3 | ||
rs1024161 | 0.925 | 0.160 | 2 | 203857029 | intergenic variant | T/A;C | snv | 2 | |||
rs2292239 | 0.742 | 0.480 | 12 | 56088396 | intron variant | T/G | snv | 0.65 | 2 | ||
rs848 | 0.807 | 0.240 | 5 | 132660808 | 3 prime UTR variant | A/C | snv | 0.67 | 2 | ||
rs3118470 | 0.752 | 0.360 | 10 | 6059750 | intron variant | T/A;C | snv | 2 | |||
rs3099844 | 0.732 | 0.400 | 6 | 31481199 | non coding transcript exon variant | C/A | snv | 0.11 | 2 | ||
rs11224294 | 0.925 | 0.080 | 11 | 100578431 | regulatory region variant | T/C | snv | 9.9E-02 | 1 | ||
rs2847266 | 1.000 | 0.040 | 18 | 12773339 | intron variant | C/T | snv | 0.69 | 1 | ||
rs4916209 | 1.000 | 0.040 | 1 | 173164350 | intergenic variant | G/A | snv | 0.33 | 1 | ||
rs6848139 | 1.000 | 0.040 | 4 | 122473886 | intergenic variant | A/C;G | snv | 1 | |||
rs7682241 | 1.000 | 0.040 | 4 | 122602720 | regulatory region variant | G/T | snv | 0.30 | 1 | ||
rs7682481 | 1.000 | 0.040 | 4 | 122602871 | regulatory region variant | G/A;C | snv | 1 | |||
rs9268528 | 0.851 | 0.280 | 6 | 32415331 | regulatory region variant | A/G | snv | 0.34 | 1 | ||
rs9479482 | 1.000 | 0.040 | 6 | 150036876 | downstream gene variant | T/C | snv | 0.36 | 1 | ||
rs3789129 | 1.000 | 0.040 | 2 | 110940463 | intron variant | A/C | snv | 0.18 | 1 | ||
rs3862469 | 1.000 | 0.040 | 16 | 11100223 | intron variant | C/T | snv | 0.35 | 1 | ||
rs231775 | 0.504 | 0.720 | 2 | 203867991 | missense variant | A/G;T | snv | 0.42; 4.0E-06 | 1 | ||
rs2216164 | 1.000 | 0.040 | 12 | 68140560 | intron variant | A/G | snv | 0.49 | 1 | ||
rs6906608 | 1.000 | 0.040 | 6 | 411554 | downstream gene variant | C/A | snv | 0.11 | 1 |