Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1250567 | 0.776 | 0.080 | 10 | 79286508 | intron variant | T/C | snv | 0.56 | 10 | ||
rs1250566 | 10 | 79286696 | intron variant | G/A | snv | 0.24 | 1 | ||||
rs1250563 | 0.724 | 0.240 | 10 | 79287626 | intron variant | G/C | snv | 0.24 | 14 | ||
rs2802372 | 10 | 79287818 | intron variant | A/C | snv | 0.44 | 1 | ||||
rs1782645 | 1.000 | 0.080 | 10 | 79288854 | intron variant | C/A;T | snv | 1 | |||
rs1250552 | 0.882 | 0.200 | 10 | 79298270 | intron variant | A/C;G | snv | 1 | |||
rs1250550 | 0.851 | 0.240 | 10 | 79300560 | intron variant | C/A | snv | 0.27 | 5 | ||
rs1250557 | 1.000 | 0.080 | 10 | 79306017 | intron variant | G/T | snv | 0.63 | 1 |