Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs16847548 | 0.807 | 0.120 | 1 | 162065484 | upstream gene variant | T/C | snv | 0.22 | 8 | ||
rs12720459 | 0.807 | 0.160 | 11 | 2583535 | missense variant | C/A;G;T | snv | 7 | |||
rs199472921 | 0.882 | 0.120 | 7 | 150951712 | missense variant | C/G;T | snv | 5 | |||
rs199472678 | 0.925 | 0.120 | 11 | 2445430 | missense variant | A/G | snv | 8.9E-06 | 3 | ||
rs2074238 | 1.000 | 0.120 | 11 | 2463573 | intron variant | T/A;C | snv | 3 |