Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2523608 | 0.925 | 0.040 | 6 | 31354782 | non coding transcript exon variant | G/A | snv | 0.19 | 5 | ||
rs9260489 | 1.000 | 0.080 | 6 | 29952555 | upstream gene variant | T/A;G | snv | 2 | |||
rs16899524 | 6 | 31394533 | non coding transcript exon variant | C/T | snv | 0.10 | 1 | ||||
rs2023472 | 6 | 30108087 | missense variant | A/C;G | snv | 4.1E-06; 0.68 | 1 | ||||
rs2596466 | 1.000 | 0.120 | 6 | 31437840 | intron variant | T/C | snv | 5.3E-02 | 1 | ||
rs9264638 | 6 | 31270541 | intron variant | G/A;C | snv | 1 | |||||
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 61 |