Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1799964 | 0.608 | 0.760 | 6 | 31574531 | upstream gene variant | T/C | snv | 0.19 | 1 | ||
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 8 | |
rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 34 | |
rs63750579 | 0.742 | 0.280 | 21 | 25891856 | missense variant | C/G;T | snv | 1 | |||
rs63750264 | 0.716 | 0.360 | 21 | 25891784 | missense variant | C/A;G;T | snv | 2 | |||
rs113209956 | 9 | 25211195 | intergenic variant | C/T | snv | 5.4E-02 | 1 | ||||
rs79928194 | 2 | 232784580 | intron variant | T/C | snv | 0.14 | 1 | ||||
rs1006737 | 0.695 | 0.120 | 12 | 2236129 | intron variant | G/A | snv | 0.36 | 7 | ||
rs4951043 | 1 | 204105737 | intron variant | C/T | snv | 0.51 | 1 | ||||
rs1192553 | 1 | 17967858 | intergenic variant | G/A | snv | 0.70 | 1 | ||||
rs4692589 | 4 | 170014094 | intron variant | A/G | snv | 0.44 | 1 | ||||
rs9875578 | 3 | 13752941 | intergenic variant | G/A;C | snv | 1 | |||||
rs72711240 | 4 | 134774652 | intron variant | C/T | snv | 2.2E-02 | 1 | ||||
rs11059336 | 12 | 127745489 | regulatory region variant | T/C | snv | 0.14 | 1 | ||||
rs10893268 | 11 | 124568716 | intron variant | C/T | snv | 0.40 | 1 | ||||
rs1143634 | 0.597 | 0.680 | 2 | 112832813 | synonymous variant | G/A | snv | 0.19 | 0.19 | 1 | |
rs11669576 | 0.851 | 0.160 | 19 | 11111624 | missense variant | G/A | snv | 4.3E-02 | 8.4E-02 | 1 | |
rs1709393 | 1.000 | 0.080 | 3 | 101980310 | intron variant | C/T | snv | 0.55 | 2 |