Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10136789 | 14 | 62889535 | intron variant | T/C | snv | 0.15 | 1 | ||||
rs10150332 | 14 | 79470621 | intron variant | T/C | snv | 0.26 | 1 | ||||
rs10261878 | 7 | 25910925 | intergenic variant | A/C | snv | 0.80 | 1 | ||||
rs10458787 | 1.000 | 0.040 | 10 | 4613373 | intergenic variant | A/C;G | snv | 2 | |||
rs10767664 | 0.752 | 0.400 | 11 | 27704439 | intron variant | T/A | snv | 0.83 | 1 | ||
rs10769908 | 11 | 8462542 | intron variant | C/T | snv | 0.55 | 1 | ||||
rs10789336 | 1 | 72372723 | intron variant | G/A;C | snv | 1 | |||||
rs10838738 | 1.000 | 0.080 | 11 | 47641497 | intron variant | A/G | snv | 0.28 | 1 | ||
rs10871777 | 0.925 | 0.120 | 18 | 60184530 | intergenic variant | A/G | snv | 0.24 | 3 | ||
rs10913469 | 1.000 | 0.080 | 1 | 177944384 | intron variant | T/C | snv | 0.22 | 3 | ||
rs10938397 | 0.851 | 0.200 | 4 | 45180510 | intergenic variant | A/G | snv | 0.37 | 8 | ||
rs10968576 | 0.882 | 0.120 | 9 | 28414341 | intron variant | A/G | snv | 0.26 | 5 | ||
rs10993160 | 9 | 94306644 | downstream gene variant | A/G | snv | 4.2E-02 | 1 | ||||
rs11030104 | 0.790 | 0.240 | 11 | 27662970 | intron variant | A/G | snv | 0.16 | 2 | ||
rs1106683 | 7 | 131768766 | intergenic variant | G/A | snv | 0.14 | 1 | ||||
rs11075990 | 0.925 | 0.120 | 16 | 53785981 | intron variant | A/G | snv | 0.41 | 1 | ||
rs11084753 | 1.000 | 0.080 | 19 | 33831232 | intergenic variant | A/C;G;T | snv | 0.65 | 1 | ||
rs11142387 | 9 | 70383416 | downstream gene variant | A/C | snv | 0.49 | 2 | ||||
rs11161721 | 1 | 86022231 | intron variant | C/A | snv | 0.27 | 0.27 | 4 | |||
rs11191580 | 0.827 | 0.040 | 10 | 103146454 | intron variant | T/C | snv | 7.9E-02 | 10 | ||
rs1121980 | 0.807 | 0.240 | 16 | 53775335 | intron variant | G/A;C | snv | 5 | |||
rs11231693 | 11 | 64095140 | intron variant | G/A | snv | 0.11 | 2 | ||||
rs113722913 | 1 | 199950846 | intergenic variant | T/C | snv | 2.6E-02 | 3 | ||||
rs11671664 | 0.925 | 0.120 | 19 | 45669020 | intron variant | G/A | snv | 0.12 | 2 | ||
rs11676272 | 1.000 | 0.040 | 2 | 24918669 | missense variant | A/G | snv | 0.47 | 0.57 | 3 |