Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1267969615 | 0.532 | 0.760 | 17 | 63490960 | missense variant | T/C | snv | 4.0E-06 | 100 | ||
rs1800764 | 0.790 | 0.320 | 17 | 63473168 | upstream gene variant | C/G;T | snv | 10 | |||
rs713041 | 0.776 | 0.400 | 19 | 1106616 | stop gained | T/A;C | snv | 4.2E-06; 0.58 | 16 | ||
rs1041740 | 0.807 | 0.320 | 21 | 31667849 | intron variant | C/T | snv | 0.24 | 8 |