Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7999279 | 1.000 | 0.200 | 13 | 47376590 | intergenic variant | A/C | snv | 0.76 | 1 | ||
rs9271573 | 1.000 | 0.200 | 6 | 32622724 | TF binding site variant | A/C | snv | 0.55 | 1 | ||
rs485497 | 0.925 | 0.200 | 3 | 160001345 | intron variant | A/C;G | snv | 2 | |||
rs8192284 | 0.724 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 19 | |||
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 | ||
rs115575857 | 1.000 | 0.200 | 6 | 32691868 | regulatory region variant | A/G | snv | 1 | |||
rs2201841 | 0.716 | 0.440 | 1 | 67228519 | intron variant | A/G;T | snv | 14 | |||
rs2431098 | 0.827 | 0.240 | 5 | 160460329 | intron variant | A/G;T | snv | 5 | |||
rs10553577 | 1.000 | 0.200 | 2 | 191090464 | intron variant | ATAATA/-;ATA;ATAATAATA | delins | 1 | |||
rs10889677 | 0.627 | 0.720 | 1 | 67259437 | 3 prime UTR variant | C/A | snv | 0.27 | 40 | ||
rs1507153 | 1.000 | 0.200 | 6 | 78774669 | intergenic variant | C/A | snv | 0.32 | 1 | ||
rs17074492 | 1.000 | 0.200 | 13 | 81587764 | intergenic variant | C/A;T | snv | 1 | |||
rs5029939 | 0.701 | 0.440 | 6 | 137874586 | intron variant | C/G | snv | 0.13 | 19 | ||
rs116855232 | 0.742 | 0.400 | 13 | 48045719 | missense variant | C/T | snv | 2.8E-02 | 1.1E-02 | 12 | |
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 | ||
rs10168266 | 0.776 | 0.400 | 2 | 191071078 | intron variant | C/T | snv | 0.19 | 8 | ||
rs774359492 | 0.807 | 0.200 | 14 | 55008684 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 7 | |
rs9277554 | 0.790 | 0.520 | 6 | 33087761 | 3 prime UTR variant | C/T | snv | 0.38 | 7 | ||
rs11805303 | 0.827 | 0.240 | 1 | 67209833 | intron variant | C/T | snv | 0.30 | 6 | ||
rs359457 | 0.925 | 0.240 | 5 | 173852839 | intergenic variant | C/T | snv | 0.59 | 2 | ||
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 | ||
rs1143634 | 0.597 | 0.680 | 2 | 112832813 | synonymous variant | G/A | snv | 0.19 | 0.19 | 52 |