Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs174621 | 1.000 | 11 | 61862632 | non coding transcript exon variant | G/A;C | snv | 2 | ||||
rs12617922 | 1.000 | 2 | 145399111 | intergenic variant | G/A | snv | 0.46 | 1 | |||
rs12788104 | 1.000 | 11 | 1129831 | regulatory region variant | A/G | snv | 0.55 | 1 | |||
rs56389811 | 1.000 | 12 | 47811575 | intron variant | C/A;T | snv | 1 | ||||
rs17454584 | 0.851 | 0.080 | 4 | 122432277 | downstream gene variant | A/G | snv | 0.17 | 6 | ||
rs117710327 | 0.882 | 0.080 | 19 | 33235672 | TF binding site variant | C/A | snv | 5.0E-02 | 5 | ||
rs2056626 | 0.882 | 0.080 | 1 | 167451188 | intron variant | T/G | snv | 0.30 | 5 | ||
rs7936312 | 0.882 | 0.080 | 11 | 76582682 | intergenic variant | G/T | snv | 0.44 | 5 | ||
rs10414065 | 0.882 | 0.080 | 19 | 33230549 | upstream gene variant | C/T | snv | 5.5E-02 | 4 | ||
rs10667251 | 0.925 | 0.080 | 17 | 49388381 | intron variant | -/TCT | delins | 0.47 | 4 | ||
rs12470864 | 0.925 | 0.080 | 2 | 102309902 | upstream gene variant | G/A | snv | 0.30 | 4 | ||
rs12722502 | 0.882 | 0.080 | 10 | 6051176 | intron variant | C/T | snv | 7.8E-03 | 4 | ||
rs3122929 | 0.882 | 0.080 | 12 | 57115319 | intron variant | C/T | snv | 0.33 | 4 | ||
rs62322662 | 0.925 | 0.080 | 4 | 122438414 | intergenic variant | A/G | snv | 5.1E-02 | 4 | ||
rs72823641 | 0.882 | 0.080 | 2 | 102319699 | intron variant | T/A;C | snv | 4 | |||
rs992969 | 0.882 | 0.080 | 9 | 6209697 | intergenic variant | A/G;T | snv | 4 | |||
rs11715524 | 0.925 | 0.080 | 3 | 196035621 | intron variant | G/A | snv | 0.54 | 3 | ||
rs1775554 | 0.882 | 0.080 | 10 | 9012377 | intergenic variant | A/C | snv | 0.35 | 3 | ||
rs10699671 | 0.925 | 0.080 | 5 | 142139375 | intron variant | -/AGG | delins | 0.68 | 2 | ||
rs10795672 | 0.925 | 0.080 | 10 | 8735677 | intergenic variant | G/A;T | snv | 2 | |||
rs11088309 | 0.925 | 0.080 | 21 | 35092334 | intron variant | C/A;G | snv | 9.3E-02 | 2 | ||
rs1117490 | 0.925 | 0.080 | 6 | 30202733 | intron variant | T/C | snv | 0.24 | 2 | ||
rs11178648 | 0.925 | 0.080 | 12 | 71139430 | intron variant | C/T | snv | 0.29 | 2 | ||
rs11255504 | 0.925 | 0.080 | 10 | 8062378 | intron variant | A/G;T | snv | 2 | |||
rs11742240 | 0.925 | 0.080 | 5 | 35881274 | downstream gene variant | G/A;T | snv | 2 |