Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1250552 | 0.882 | 0.200 | 10 | 79298270 | intron variant | A/C;G | snv | 5 | |||
rs1250550 | 0.851 | 0.240 | 10 | 79300560 | intron variant | C/A | snv | 0.27 | 3 | ||
rs1250546 | 0.925 | 0.080 | 10 | 79272775 | intron variant | A/G | snv | 0.36 | 2 | ||
rs704010 | 0.851 | 0.080 | 10 | 79081391 | intron variant | T/C | snv | 0.71 | 1 | ||
rs12571751 | 0.925 | 0.120 | 10 | 79182874 | intron variant | A/G | snv | 0.46 | 1 | ||
rs1749824 | 0.925 | 0.080 | 10 | 79164105 | intron variant | C/A | snv | 0.39 | 1 | ||
rs1250542 | 1.000 | 0.080 | 10 | 79274913 | intron variant | G/A | snv | 0.32 | 1 | ||
rs1250544 | 0.882 | 0.080 | 10 | 79273128 | intron variant | G/A | snv | 0.32 | 1 | ||
rs11593576 | 0.925 | 0.040 | 10 | 79256139 | intron variant | C/T | snv | 0.29 | 1 | ||
rs780151 | 10 | 79171724 | intron variant | G/A | snv | 0.32 | 1 | ||||
rs7916441 | 10 | 79165820 | intron variant | G/C | snv | 0.39 | 1 |