Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs649775 | 0.882 | 0.120 | 6 | 33716536 | upstream gene variant | A/G;T | snv | 3 | |||
rs1040411 | 1.000 | 0.120 | 6 | 106150148 | intron variant | G/A | snv | 0.47 | 3 | ||
rs4946728 | 1.000 | 0.120 | 6 | 106142488 | intron variant | A/C | snv | 0.72 | 3 | ||
rs1860661 | 0.882 | 0.120 | 19 | 1650135 | intron variant | A/C;G | snv | 6.7E-06; 0.54 | 3 |