Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7574865 | 0.574 | 0.720 | 2 | 191099907 | intron variant | T/G | snv | 0.79 | 59 | ||
rs5029939 | 0.701 | 0.440 | 6 | 137874586 | intron variant | C/G | snv | 0.13 | 19 | ||
rs7517847 | 0.689 | 0.600 | 1 | 67215986 | intron variant | T/G | snv | 0.37 | 19 | ||
rs2201841 | 0.716 | 0.440 | 1 | 67228519 | intron variant | A/G;T | snv | 14 | |||
rs11889341 | 0.732 | 0.480 | 2 | 191079016 | intron variant | C/T | snv | 0.21 | 12 | ||
rs117026326 | 0.752 | 0.440 | 7 | 74711703 | intron variant | C/T | snv | 1.3E-02 | 10 | ||
rs1004819 | 0.776 | 0.360 | 1 | 67204530 | intron variant | G/A | snv | 0.30 | 9 | ||
rs10168266 | 0.776 | 0.400 | 2 | 191071078 | intron variant | C/T | snv | 0.19 | 8 | ||
rs11805303 | 0.827 | 0.240 | 1 | 67209833 | intron variant | C/T | snv | 0.30 | 6 | ||
rs4282438 | 0.807 | 0.280 | 6 | 33104395 | intron variant | T/G | snv | 3.1E-02 | 6 | ||
rs7341475 | 0.851 | 0.240 | 7 | 103764368 | intron variant | G/A | snv | 0.17 | 6 | ||
rs10489629 | 0.827 | 0.240 | 1 | 67222666 | intron variant | T/C | snv | 0.48 | 5 | ||
rs2431098 | 0.827 | 0.240 | 5 | 160460329 | intron variant | A/G;T | snv | 5 | |||
rs3135394 | 0.851 | 0.240 | 6 | 32440720 | intron variant | A/G | snv | 6.3E-02 | 4 | ||
rs2736345 | 0.882 | 0.280 | 8 | 11494976 | intron variant | A/G | snv | 0.35 | 3 | ||
rs3823536 | 0.925 | 0.280 | 7 | 128939612 | intron variant | G/A | snv | 0.40 | 2 | ||
rs485497 | 0.925 | 0.200 | 3 | 160001345 | intron variant | A/C;G | snv | 2 | |||
rs10553577 | 1.000 | 0.200 | 2 | 191090464 | intron variant | ATAATA/-;ATA;ATAATAATA | delins | 1 | |||
rs11048434 | 1.000 | 0.200 | 12 | 9001336 | intron variant | G/A | snv | 0.28 | 1 | ||
rs17339836 | 1.000 | 0.200 | 7 | 129041008 | intron variant | C/T | snv | 9.0E-02 | 1 | ||
rs1957173 | 1.000 | 0.200 | 14 | 45937713 | intron variant | C/T | snv | 4.6E-02 | 1 | ||
rs6579837 | 1.000 | 0.200 | 5 | 151055333 | intron variant | G/T | snv | 0.11 | 1 | ||
rs6933404 | 0.925 | 0.280 | 6 | 137638098 | intergenic variant | T/C | snv | 0.16 | 5 | ||
rs359457 | 0.925 | 0.240 | 5 | 173852839 | intergenic variant | C/T | snv | 0.59 | 2 | ||
rs1507153 | 1.000 | 0.200 | 6 | 78774669 | intergenic variant | C/A | snv | 0.32 | 1 |