Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3771829 | 0.790 | 0.120 | 2 | 75137019 | intron variant | C/G | snv | 0.11 | 9 | ||
rs1106854 | 0.827 | 0.080 | 2 | 75050887 | intron variant | T/C;G | snv | 5 | |||
rs4290270 | 0.724 | 0.320 | 12 | 72022455 | synonymous variant | A/T | snv | 0.57 | 0.55 | 17 | |
rs1386483 | 0.790 | 0.080 | 12 | 72018714 | intron variant | T/C | snv | 0.53 | 9 | ||
rs17110563 | 0.827 | 0.080 | 12 | 71972526 | missense variant | C/T | snv | 1.2E-03 | 1.1E-03 | 7 | |
rs1386482 | 0.827 | 0.080 | 12 | 72018792 | intron variant | T/G | snv | 0.52 | 5 | ||
rs1386486 | 0.827 | 0.080 | 12 | 72018440 | intron variant | A/G | snv | 0.53 | 5 | ||
rs2812393 | 0.807 | 0.080 | 1 | 231777927 | intron variant | G/C | snv | 0.61 | 6 | ||
rs766288 | 0.790 | 0.080 | 1 | 231557942 | intron variant | G/T | snv | 0.40 | 7 |