Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
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 | |||
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 | ||
rs992969 | 0.882 | 0.080 | 9 | 6209697 | intergenic variant | A/G;T | snv | 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 | |||
rs1321859 | 0.925 | 0.080 | 6 | 90301954 | intron variant | C/T | snv | 0.24 | 2 | ||
rs17668708 | 0.925 | 0.080 | 1 | 198671359 | intron variant | C/T | snv | 8.0E-02 | 2 | ||
rs1784775 | 0.925 | 0.080 | 11 | 111601736 | upstream gene variant | T/C | snv | 0.59 | 2 | ||
rs190438685 | 0.925 | 0.080 | 4 | 39388825 | intergenic variant | C/T | snv | 6.2E-03 | 2 | ||
rs2056625 | 0.925 | 0.080 | 1 | 167451062 | intron variant | G/A | snv | 0.27 | 2 | ||
rs2056626 | 0.882 | 0.080 | 1 | 167451188 | intron variant | T/G | snv | 0.30 | 2 | ||
rs2381712 | 0.925 | 0.080 | 2 | 145387450 | intergenic variant | T/G | snv | 0.52 | 2 | ||
rs2544026 | 0.925 | 0.080 | 12 | 47792780 | non coding transcript exon variant | T/A | snv | 0.19 | 2 | ||
rs28407950 | 0.925 | 0.080 | 6 | 32658571 | upstream gene variant | C/T | snv | 0.29 | 2 | ||
rs28415845 | 0.925 | 0.080 | 11 | 1151933 | regulatory region variant | T/C | snv | 0.58 | 2 | ||
rs28635831 | 0.925 | 0.080 | 13 | 39745817 | intron variant | A/G | snv | 0.27 | 2 | ||
rs3024655 | 0.925 | 0.080 | 16 | 27358181 | intron variant | A/G;T | snv | 2 |