Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 61 | ||
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 55 | |
rs28929474 | 0.708 | 0.320 | 14 | 94378610 | missense variant | C/G;T | snv | 2.8E-05; 1.1E-02 | 17 | ||
rs12740374 | 0.851 | 0.040 | 1 | 109274968 | 3 prime UTR variant | G/T | snv | 0.22 | 9 | ||
rs5112 | 1.000 | 0.080 | 19 | 44927023 | non coding transcript exon variant | C/G | snv | 0.55 | 4 | ||
rs6234 | 0.851 | 0.160 | 5 | 96393270 | missense variant | G/C | snv | 0.27 | 0.24 | 4 | |
rs45446698 | 0.807 | 0.120 | 7 | 99735325 | upstream gene variant | T/G | snv | 2.7E-02 | 3 | ||
rs11599750 | 10 | 100045685 | intron variant | C/T | snv | 0.40 | 2 | ||||
rs12408663 | 1 | 19641564 | intron variant | T/C | snv | 0.19 | 2 | ||||
rs12964 | 12 | 6463025 | 3 prime UTR variant | T/C | snv | 0.46 | 2 | ||||
rs182722517 | 19 | 50739310 | TF binding site variant | G/A | snv | 3.6E-03 | 2 | ||||
rs2249350 | 1.000 | 0.080 | 21 | 26950187 | intron variant | C/A | snv | 9.7E-02 | 2 | ||
rs2270894 | 3 | 9933702 | intron variant | C/G | snv | 0.19 | 2 | ||||
rs6457374 | 0.851 | 0.200 | 6 | 31304484 | intron variant | C/T | snv | 0.81 | 2 |