Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs146052672 | 0.851 | 0.160 | 6 | 34242693 | intron variant | -/C | delins | 5 | |||
rs1467568 | 0.776 | 0.320 | 10 | 67915401 | intron variant | A/G | snv | 0.46 | 8 | ||
rs1501299 | 0.597 | 0.720 | 3 | 186853334 | intron variant | G/C;T | snv | 52 | |||
rs1544410 | 0.542 | 0.760 | 12 | 47846052 | intron variant | C/A;G;T | snv | 78 | |||
rs1550805 | 0.925 | 0.120 | 5 | 68287979 | intron variant | C/T | snv | 6.9E-02 | 2 | ||
rs1558902 | 0.827 | 0.120 | 16 | 53769662 | intron variant | T/A | snv | 0.31 | 21 | ||
rs16861329 | 0.882 | 0.160 | 3 | 186948673 | intron variant | C/T | snv | 0.13 | 3 | ||
rs17817449 | 0.716 | 0.560 | 16 | 53779455 | intron variant | T/A;G | snv | 21 | |||
rs17817964 | 0.925 | 0.120 | 16 | 53794154 | intron variant | C/T | snv | 0.30 | 6 | ||
rs1799774 | 0.882 | 0.200 | 6 | 131882331 | intron variant | T/- | delins | 3 | |||
rs1800795 | 0.494 | 0.840 | 7 | 22727026 | intron variant | C/G | snv | 0.71 | 140 | ||
rs182052 | 0.701 | 0.440 | 3 | 186842993 | intron variant | G/A | snv | 0.38 | 19 | ||
rs1968482 | 0.925 | 0.120 | 2 | 24863989 | intron variant | T/C | snv | 0.32 | 2 | ||
rs206936 | 0.882 | 0.160 | 6 | 34335092 | intron variant | A/G | snv | 0.34 | 8 | ||
rs2072907 | 0.882 | 0.120 | 22 | 43936773 | intron variant | C/G | snv | 0.20 | 3 | ||
rs2236242 | 0.776 | 0.280 | 14 | 94493715 | intron variant | T/A | snv | 0.31 | 9 | ||
rs2237892 | 0.790 | 0.320 | 11 | 2818521 | intron variant | C/T | snv | 9.2E-02 | 16 | ||
rs2237895 | 0.790 | 0.240 | 11 | 2835964 | intron variant | A/C;T | snv | 10 | |||
rs2239179 | 0.790 | 0.200 | 12 | 47863983 | intron variant | T/C | snv | 0.39 | 9 | ||
rs225011 | 0.925 | 0.120 | 14 | 80205865 | intron variant | T/A;C | snv | 2 | |||
rs2282679 | 0.645 | 0.480 | 4 | 71742666 | intron variant | T/G | snv | 0.21 | 38 | ||
rs2302870 | 0.925 | 0.120 | 2 | 207088682 | intron variant | T/C;G | snv | 2 | |||
rs2568958 | 0.882 | 0.160 | 1 | 72299433 | intron variant | G/A;C | snv | 8 | |||
rs290487 | 0.776 | 0.280 | 10 | 113149972 | intron variant | C/T | snv | 0.16 | 10 | ||
rs361072 | 0.882 | 0.120 | 3 | 138759702 | intron variant | G/A;C | snv | 4 |