Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2075650 | 0.662 | 0.360 | 19 | 44892362 | intron variant | A/G | snv | 0.13 | 0.13 | 20 | |
rs4420638 | 0.708 | 0.520 | 19 | 44919689 | downstream gene variant | A/G | snv | 0.18 | 15 | ||
rs2074356 | 0.763 | 0.280 | 12 | 112207597 | intron variant | G/A | snv | 3.8E-03 | 12 | ||
rs9939609 | 0.559 | 0.720 | 16 | 53786615 | intron variant | T/A | snv | 0.41 | 10 | ||
rs1121980 | 0.807 | 0.240 | 16 | 53775335 | intron variant | G/A;C | snv | 9 | |||
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 8 | ||
rs1883025 | 0.807 | 0.120 | 9 | 104902020 | intron variant | C/T | snv | 0.28 | 7 | ||
rs7138803 | 0.827 | 0.240 | 12 | 49853685 | intergenic variant | G/A;T | snv | 6 | |||
rs9940128 | 0.851 | 0.120 | 16 | 53766842 | intron variant | G/A | snv | 0.42 | 6 | ||
rs1051921 | 0.925 | 0.120 | 7 | 73593613 | 3 prime UTR variant | G/A | snv | 0.15 | 6 | ||
rs13389219 | 1.000 | 0.080 | 2 | 164672366 | intron variant | C/T | snv | 0.47 | 5 | ||
rs9930506 | 0.776 | 0.360 | 16 | 53796553 | intron variant | A/G | snv | 0.36 | 5 | ||
rs8070723 | 0.851 | 0.240 | 17 | 46003698 | intron variant | A/G | snv | 0.18 | 5 | ||
rs7498665 | 0.925 | 0.120 | 16 | 28871920 | missense variant | A/G;T | snv | 0.35 | 5 | ||
rs10808546 | 8 | 125483576 | intron variant | C/T | snv | 0.39 | 4 | ||||
rs605066 | 6 | 139508529 | intron variant | C/T | snv | 0.53 | 4 | ||||
rs998584 | 6 | 43790159 | downstream gene variant | C/A | snv | 0.41 | 4 | ||||
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 4 | |
rs12936587 | 0.882 | 0.080 | 17 | 17640408 | regulatory region variant | G/A | snv | 0.38 | 3 | ||
rs13130484 | 1.000 | 0.080 | 4 | 45173674 | intergenic variant | C/A;T | snv | 3 | |||
rs6567160 | 1.000 | 0.080 | 18 | 60161902 | upstream gene variant | T/C | snv | 0.21 | 3 | ||
rs727428 | 0.882 | 0.200 | 17 | 7634474 | downstream gene variant | T/C | snv | 0.55 | 3 | ||
rs887912 | 1.000 | 0.080 | 2 | 59075742 | intron variant | T/C;G | snv | 3 | |||
rs6795735 | 0.882 | 0.120 | 3 | 64719689 | intron variant | C/A;G;T | snv | 3 | |||
rs9931989 | 16 | 28894763 | intron variant | G/C | snv | 0.68 | 3 |