Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4444235 | 0.701 | 0.240 | 14 | 53944201 | downstream gene variant | T/C | snv | 0.43 | 15 | ||
rs16892766 | 0.716 | 0.240 | 8 | 116618444 | intergenic variant | A/C | snv | 9.3E-02 | 10 | ||
rs4779584 | 0.732 | 0.160 | 15 | 32702555 | intergenic variant | T/C | snv | 0.67 | 8 | ||
rs961253 | 0.732 | 0.240 | 20 | 6423634 | intergenic variant | C/A | snv | 0.34 | 7 | ||
rs1321311 | 0.742 | 0.160 | 6 | 36655123 | regulatory region variant | C/A | snv | 0.28 | 6 | ||
rs7679673 | 0.677 | 0.440 | 4 | 105140377 | intron variant | C/A | snv | 0.50 | 5 | ||
rs6691170 | 0.776 | 0.080 | 1 | 221872104 | intergenic variant | G/T | snv | 0.34 | 4 | ||
rs7931342 | 0.689 | 0.360 | 11 | 69227030 | intergenic variant | T/G | snv | 0.58 | 4 | ||
rs11255841 | 0.776 | 0.080 | 10 | 8697617 | intergenic variant | T/A | snv | 0.25 | 3 | ||
rs12970291 | 0.763 | 0.120 | 18 | 75305279 | intergenic variant | G/A | snv | 2.8E-02 | 3 | ||
rs6687758 | 0.763 | 0.200 | 1 | 221991606 | regulatory region variant | A/G | snv | 0.20 | 3 | ||
rs11903757 | 0.763 | 0.160 | 2 | 191722478 | intron variant | T/C | snv | 0.16 | 2 | ||
rs16969681 | 0.776 | 0.080 | 15 | 32700910 | downstream gene variant | C/T | snv | 0.11 | 2 | ||
rs2965667 | 0.776 | 0.080 | 12 | 17291799 | intergenic variant | A/T | snv | 0.96 | 2 | ||
rs4813802 | 0.776 | 0.080 | 20 | 6718948 | regulatory region variant | T/G | snv | 0.28 | 2 | ||
rs1035209 | 0.790 | 0.080 | 10 | 99585609 | intergenic variant | C/T | snv | 0.15 | 1 | ||
rs1367374 | 0.790 | 0.080 | 2 | 153074663 | intergenic variant | G/C | snv | 0.19 | 1 | ||
rs16941835 | 0.790 | 0.080 | 16 | 86662114 | intron variant | G/C | snv | 0.20 | 1 | ||
rs2423279 | 0.790 | 0.080 | 20 | 7831703 | downstream gene variant | T/C | snv | 0.29 | 1 | ||
rs6061231 | 0.790 | 0.080 | 20 | 62381861 | downstream gene variant | C/A | snv | 0.28 | 1 | ||
rs6469656 | 0.790 | 0.080 | 8 | 116635549 | regulatory region variant | G/A;C | snv | 1 | |||
rs72647484 | 0.790 | 0.080 | 1 | 22261235 | regulatory region variant | T/C | snv | 6.2E-02 | 1 | ||
rs964293 | 0.790 | 0.080 | 20 | 54200178 | TF binding site variant | C/A;T | snv | 1 | |||
rs1254244346 | 1.000 | 0.080 | 9 | 104822502 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
rs11169552 | 0.776 | 0.080 | 12 | 50761880 | upstream gene variant | C/T | snv | 0.23 | 2 |