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 | ||
rs2234693 | 0.555 | 0.680 | 6 | 151842200 | intron variant | T/C | snv | 0.47 | 77 | ||
rs6280 | 0.602 | 0.520 | 3 | 114171968 | missense variant | C/T | snv | 0.63 | 0.54 | 57 | |
rs12778366 | 0.724 | 0.480 | 10 | 67883321 | upstream gene variant | T/C;G | snv | 13 | |||
rs3213207 | 0.776 | 0.120 | 6 | 15627871 | intron variant | T/C | snv | 8.7E-02 | 11 | ||
rs10997875 | 0.882 | 0.080 | 10 | 67920067 | downstream gene variant | T/A;C | snv | 4 | |||
rs6693503 | 1.000 | 0.040 | 1 | 19660801 | upstream gene variant | A/G | snv | 0.55 | 1 | ||
rs4912138 | 1.000 | 0.040 | 1 | 19666992 | intron variant | A/G;T | snv | 1 |