Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs780159 | 10 | 79147390 | intron variant | A/C;G | snv | 2 | |||||
rs1250546 | 0.925 | 0.080 | 10 | 79272775 | intron variant | A/G | snv | 0.36 | 3 | ||
rs1250544 | 0.882 | 0.080 | 10 | 79273128 | intron variant | G/A | snv | 0.32 | 3 | ||
rs703978 | 1.000 | 0.080 | 10 | 79184390 | intron variant | C/G;T | snv | 0.68 | 3 | ||
rs1250573 | 0.827 | 0.120 | 10 | 79282718 | intron variant | G/A | snv | 0.23 | 5 | ||
rs1250550 | 0.851 | 0.240 | 10 | 79300560 | intron variant | C/A | snv | 0.27 | 5 | ||
rs1250567 | 0.776 | 0.080 | 10 | 79286508 | intron variant | T/C | snv | 0.56 | 10 | ||
rs1250563 | 0.724 | 0.240 | 10 | 79287626 | intron variant | G/C | snv | 0.24 | 14 |