Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
rs104893877 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 59 | |||
rs74315401 | 0.683 | 0.320 | 20 | 4699525 | missense variant | C/T | snv | 32 | |||
rs646776 | 0.752 | 0.240 | 1 | 109275908 | downstream gene variant | C/T | snv | 0.74 | 25 | ||
rs104893878 | 0.732 | 0.160 | 4 | 89835580 | missense variant | C/G | snv | 21 | |||
rs5848 | 0.708 | 0.120 | 17 | 44352876 | 3 prime UTR variant | C/T | snv | 0.41 | 17 | ||
rs1990622 | 0.742 | 0.200 | 7 | 12244161 | downstream gene variant | A/G | snv | 0.52 | 16 | ||
rs63751438 | 0.776 | 0.120 | 17 | 46010388 | missense variant | C/T | snv | 16 | |||
rs121912443 | 0.732 | 0.160 | 21 | 31663857 | missense variant | A/G | snv | 15 | |||
rs104894201 | 0.763 | 0.280 | 11 | 111908934 | missense variant | T/C | snv | 12 | |||
rs104893768 | 0.807 | 0.080 | 3 | 129528801 | missense variant | C/A | snv | 11 | |||
rs121909329 | 0.763 | 0.200 | 9 | 35065363 | missense variant | C/A;G;T | snv | 11 | |||
rs431905511 | 0.827 | 0.080 | 4 | 89828154 | missense variant | C/T | snv | 9 | |||
rs63750311 | 0.790 | 0.240 | 14 | 73192647 | missense variant | A/C | snv | 8 | |||
rs63750570 | 0.827 | 0.120 | 17 | 46018629 | missense variant | G/A | snv | 8 | |||
rs35801418 | 0.827 | 0.120 | 12 | 40321114 | missense variant | A/G | snv | 7 | |||
rs63750376 | 0.827 | 0.120 | 17 | 45996657 | missense variant | G/T | snv | 7 | |||
rs63751068 | 0.827 | 0.120 | 14 | 73186920 | missense variant | G/C;T | snv | 6 | |||
rs766001707 | 0.851 | 0.200 | 14 | 92096772 | missense variant | C/T | snv | 6 | |||
rs2435200 | 0.925 | 0.080 | 17 | 45994485 | intron variant | G/A | snv | 0.40 | 5 | ||
rs1178466848 | 0.925 | 0.120 | 20 | 4699785 | missense variant | G/A | snv | 2.8E-05 | 4 | ||
rs119467003 | 0.882 | 0.080 | 14 | 89993420 | missense variant | A/G | snv | 2.1E-05 | 4 | ||
rs66468541 | 0.925 | 0.080 | 2 | 197497275 | missense variant | C/T | snv | 4 | |||
rs104893922 | 0.925 | 0.080 | 5 | 70946157 | missense variant | A/G | snv | 3 | |||
rs1272951905 | 0.925 | 0.160 | 16 | 86532210 | missense variant | C/T | snv | 2.1E-05 | 3 |