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 | |
rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
rs1017412 | 1.000 | 0.040 | 15 | 87868912 | 3 prime UTR variant | G/A;C | snv | 1 | |||
rs7176429 | 1.000 | 0.040 | 15 | 87876193 | 3 prime UTR variant | T/A;G | snv | 1 |