Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs540485182 | 0.925 | 0.080 | 5 | 110825774 | intergenic variant | -/A;AA;AAA | delins | 2 | |||
rs10699671 | 0.925 | 0.080 | 5 | 142139375 | intron variant | -/AGG | delins | 0.68 | 2 | ||
rs10667251 | 0.925 | 0.080 | 17 | 49388381 | intron variant | -/TCT | delins | 0.47 | 4 | ||
rs35204956 | 0.925 | 0.080 | 8 | 80389778 | intron variant | A/-;AA;AAA | delins | 2 | |||
rs1342326 | 0.790 | 0.360 | 9 | 6190076 | intergenic variant | A/C | snv | 0.21 | 9 | ||
rs1775554 | 0.882 | 0.080 | 10 | 9012377 | intergenic variant | A/C | snv | 0.35 | 3 | ||
rs7183955 | 0.925 | 0.080 | 15 | 60757370 | intron variant | A/C | snv | 0.24 | 2 | ||
rs1800797 | 0.605 | 0.800 | 7 | 22726602 | non coding transcript exon variant | A/G | snv | 0.72 | 43 | ||
rs17622378 | 0.790 | 0.200 | 5 | 132442760 | intron variant | A/G | snv | 0.28 | 8 | ||
rs17454584 | 0.851 | 0.080 | 4 | 122432277 | downstream gene variant | A/G | snv | 0.17 | 6 | ||
rs62322662 | 0.925 | 0.080 | 4 | 122438414 | intergenic variant | A/G | snv | 5.1E-02 | 4 | ||
rs28635831 | 0.925 | 0.080 | 13 | 39745817 | intron variant | A/G | snv | 0.27 | 2 | ||
rs6866614 | 0.925 | 0.080 | 5 | 132451445 | intron variant | A/G | snv | 0.71 | 2 | ||
rs12788104 | 1.000 | 11 | 1129831 | regulatory region variant | A/G | snv | 0.55 | 1 | |||
rs992969 | 0.882 | 0.080 | 9 | 6209697 | intergenic variant | A/G;T | snv | 4 | |||
rs11255504 | 0.925 | 0.080 | 10 | 8062378 | intron variant | A/G;T | snv | 2 | |||
rs3024655 | 0.925 | 0.080 | 16 | 27358181 | intron variant | A/G;T | snv | 2 | |||
rs58521088 | 0.925 | 0.080 | 6 | 90275479 | intron variant | A/T | snv | 0.27 | 2 | ||
rs117710327 | 0.882 | 0.080 | 19 | 33235672 | TF binding site variant | C/A | snv | 5.0E-02 | 5 | ||
rs11088309 | 0.925 | 0.080 | 21 | 35092334 | intron variant | C/A;G | snv | 9.3E-02 | 2 | ||
rs72743461 | 0.827 | 0.160 | 15 | 67149412 | intron variant | C/A;T | snv | 6 | |||
rs56389811 | 1.000 | 12 | 47811575 | intron variant | C/A;T | snv | 1 | ||||
rs7216389 | 0.732 | 0.440 | 17 | 39913696 | intron variant | C/T | snv | 0.60 | 14 | ||
rs56062135 | 0.790 | 0.200 | 15 | 67163292 | intron variant | C/T | snv | 0.18 | 8 | ||
rs11650680 | 0.827 | 0.120 | 17 | 40422984 | intergenic variant | C/T | snv | 0.17 | 5 |