Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
rs4680 | 0.442 | 0.920 | 22 | 19963748 | missense variant | G/A | snv | 0.46 | 0.44 | 249 | |
rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
rs1800497 | 0.620 | 0.400 | 11 | 113400106 | missense variant | G/A | snv | 0.26 | 0.26 | 56 | |
rs1049353 | 0.630 | 0.600 | 6 | 88143916 | synonymous variant | C/T | snv | 0.21 | 0.20 | 42 | |
rs6311 | 0.645 | 0.640 | 13 | 46897343 | upstream gene variant | C/T | snv | 0.40 | 41 | ||
rs893924483 | 0.716 | 0.280 | 11 | 27658285 | missense variant | C/A;T | snv | 4.0E-06 | 1.4E-05 | 23 | |
rs1344706 | 0.701 | 0.160 | 2 | 184913701 | intron variant | A/C;T | snv | 21 | |||
rs2023239 | 0.724 | 0.160 | 6 | 88150763 | intron variant | T/C | snv | 0.21 | 20 | ||
rs2494732 | 0.763 | 0.240 | 14 | 104772855 | intron variant | T/C | snv | 0.50 | 0.47 | 11 | |
rs1076560 | 0.776 | 0.120 | 11 | 113412966 | intron variant | C/A | snv | 0.16 | 11 | ||
rs2020936 | 0.776 | 0.160 | 17 | 30223796 | intron variant | G/A;C | snv | 10 | |||
rs2295633 | 0.827 | 0.120 | 1 | 46408711 | intron variant | A/G;T | snv | 7 | |||
rs4916723 | 0.925 | 0.040 | 5 | 88558577 | intron variant | A/C;G;T | snv | 4 | |||
rs2391769 | 0.925 | 0.040 | 1 | 96513405 | regulatory region variant | A/G;T | snv | 3 | |||
rs4259397 | 0.925 | 0.040 | 8 | 92354062 | upstream gene variant | G/A;T | snv | 2 | |||
rs4858253 | 0.925 | 0.040 | 3 | 20687599 | intron variant | C/T | snv | 0.33 | 2 | ||
rs74760947 | 0.925 | 0.040 | 8 | 34495092 | intergenic variant | A/G | snv | 3.1E-02 | 2 | ||
rs797267 | 0.925 | 0.040 | 12 | 89373460 | intron variant | A/G | snv | 0.28 | 2 | ||
rs2875907 | 0.925 | 0.040 | 3 | 85469430 | intron variant | A/G;T | snv | 2 | |||
rs806374 | 0.925 | 0.080 | 6 | 88147601 | intron variant | T/C | snv | 0.37 | 2 | ||
rs1476535 | 0.925 | 0.040 | 7 | 114430980 | intron variant | C/G;T | snv | 2 | |||
rs2189012 | 0.925 | 0.040 | 7 | 114571857 | intron variant | G/A | snv | 0.73 | 2 | ||
rs56319043 | 0.925 | 0.040 | 1 | 43705540 | intron variant | C/T | snv | 0.17 | 2 | ||
rs139868495 | 0.925 | 0.040 | 8 | 34805452 | intron variant | C/T | snv | 3.1E-02 | 2 |