Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 24 | ||
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 | ||
rs8050136 | 0.716 | 0.560 | 16 | 53782363 | intron variant | C/A | snv | 0.40 | 11 | ||
rs12229654 | 0.763 | 0.320 | 12 | 110976657 | intergenic variant | T/G | snv | 4.8E-03 | 10 | ||
rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 10 | |
rs9939609 | 0.559 | 0.720 | 16 | 53786615 | intron variant | T/A | snv | 0.41 | 10 | ||
rs2068834 | 0.925 | 0.120 | 2 | 27616672 | intron variant | T/C | snv | 0.28 | 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 | ||
rs1421085 | 0.752 | 0.280 | 16 | 53767042 | intron variant | T/C | snv | 0.31 | 7 | ||
rs17782313 | 0.683 | 0.480 | 18 | 60183864 | intergenic variant | T/C | snv | 0.24 | 6 | ||
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 | ||
rs10938397 | 0.851 | 0.200 | 4 | 45180510 | intergenic variant | A/G | snv | 0.37 | 5 | ||
rs12970134 | 0.790 | 0.280 | 18 | 60217517 | intergenic variant | G/A | snv | 0.21 | 5 | ||
rs9368222 | 1.000 | 0.080 | 6 | 20686765 | intron variant | C/A;T | snv | 5 | |||
rs4704220 | 5 | 75461731 | intron variant | G/A | snv | 0.55 | 5 | ||||
rs11075990 | 0.925 | 0.120 | 16 | 53785981 | intron variant | A/G | snv | 0.41 | 5 | ||
rs17817449 | 0.716 | 0.560 | 16 | 53779455 | intron variant | T/A;G | snv | 5 | |||
rs17817964 | 0.925 | 0.120 | 16 | 53794154 | intron variant | C/T | snv | 0.30 | 5 | ||
rs7202116 | 0.882 | 0.120 | 16 | 53787703 | intron variant | A/G | snv | 0.41 | 5 | ||
rs9930506 | 0.776 | 0.360 | 16 | 53796553 | intron variant | A/G | snv | 0.36 | 5 | ||
rs2568958 | 0.882 | 0.160 | 1 | 72299433 | intron variant | G/A;C | snv | 5 | |||
rs10913469 | 1.000 | 0.080 | 1 | 177944384 | intron variant | T/C | snv | 0.22 | 5 |