Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1689510 | 0.724 | 0.240 | 12 | 56002984 | non coding transcript exon variant | G/C | snv | 0.25 | 16 | ||
rs174535 | 0.776 | 0.280 | 11 | 61783884 | missense variant | T/A;C;G | snv | 0.38 | 0.32 | 11 | |
rs4129267 | 0.807 | 0.200 | 1 | 154453788 | intron variant | C/G;T | snv | 10 | |||
rs4845604 | 0.776 | 0.200 | 1 | 151829204 | intron variant | G/A;C;T | snv | 10 | |||
rs2497318 | 0.827 | 0.120 | 10 | 92672243 | upstream gene variant | C/A;T | snv | 6 |