Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs704010 | 0.851 | 0.080 | 10 | 79081391 | intron variant | T/C | snv | 0.71 | 1 | ||
rs1268974 | 1.000 | 0.080 | 10 | 79092621 | intron variant | A/G | snv | 0.65 | 1 | ||
rs1250573 | 0.827 | 0.120 | 10 | 79282718 | intron variant | G/A | snv | 0.23 | 5 | ||
rs12571751 | 0.925 | 0.120 | 10 | 79182874 | intron variant | A/G | snv | 0.46 | 1 | ||
rs10128264 | 1.000 | 0.120 | 10 | 79200216 | intron variant | T/C | snv | 0.64 | 1 | ||
rs1250552 | 0.882 | 0.200 | 10 | 79298270 | intron variant | A/C;G | snv | 1 | |||
rs1250563 | 0.724 | 0.240 | 10 | 79287626 | intron variant | G/C | snv | 0.24 | 14 | ||
rs1250550 | 0.851 | 0.240 | 10 | 79300560 | intron variant | C/A | snv | 0.27 | 5 |