Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs35928002 | 19 | 18005335 | intron variant | A/G | snv | 0.45 | 2 | ||||
rs4808737 | 19 | 18006837 | intron variant | C/T | snv | 0.31 | 1 | ||||
rs12981683 | 19 | 18003191 | intron variant | C/G;T | snv | 1 | |||||
rs10411508 | 19 | 17999765 | 3 prime UTR variant | G/A | snv | 0.35 | 1 |