Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11681351 | 0.925 | 0.120 | 2 | 27520556 | intron variant | G/A | snv | 0.36 | 3 | ||
rs13472 | 0.925 | 0.120 | 2 | 27377372 | 3 prime UTR variant | G/A | snv | 0.38 | 3 | ||
rs2293572 | 0.925 | 0.120 | 2 | 27505910 | intron variant | C/G | snv | 0.39 | 3 | ||
rs4665963 | 0.925 | 0.120 | 2 | 27305824 | splice region variant | T/C | snv | 0.35 | 0.43 | 3 | |
rs1528533 | 0.925 | 0.120 | 2 | 27372889 | non coding transcript exon variant | G/C | snv | 0.47 | 3 | ||
rs813592 | 0.925 | 0.120 | 2 | 27499104 | intron variant | T/C | snv | 0.42 | 0.47 | 3 | |
rs1049817 | 0.925 | 0.120 | 2 | 27328100 | synonymous variant | A/G | snv | 0.42 | 0.48 | 3 | |
rs7586601 | 0.925 | 0.120 | 2 | 27361799 | intron variant | A/G | snv | 0.54 | 3 | ||
rs1260333 | 0.882 | 0.160 | 2 | 27525757 | downstream gene variant | A/G | snv | 0.58 | 8 | ||
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 24 | ||
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 25 | |
rs780093 | 0.763 | 0.240 | 2 | 27519736 | intron variant | T/C | snv | 0.68 | 13 |