Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4887063 | 15 | 78547373 | intron variant | C/T | snv | 0.66 | 1 | ||||
rs12907966 | 15 | 78550709 | 3 prime UTR variant | C/T | snv | 0.31 | 1 | ||||
rs4887064 | 15 | 78550505 | 3 prime UTR variant | G/C | snv | 0.66 | 1 | ||||
rs905740 | 15 | 78552044 | 3 prime UTR variant | T/C | snv | 0.66 | 1 | ||||
rs3813570 | 15 | 78540490 | 5 prime UTR variant | T/C | snv | 0.27 | 1 | ||||
rs7164030 | 15 | 78552319 | 3 prime UTR variant | G/A | snv | 0.66 | 1 | ||||
rs4243083 | 15 | 78541488 | non coding transcript exon variant | C/A;G;T | snv | 1 | |||||
rs1979907 | 15 | 78549897 | 3 prime UTR variant | T/C | snv | 0.66 | 1 | ||||
rs1979905 | 15 | 78550032 | 3 prime UTR variant | A/C | snv | 0.66 | 1 | ||||
rs3813571 | 1.000 | 0.080 | 15 | 78540450 | 5 prime UTR variant | G/T | snv | 0.32 | 1 | ||
rs880395 | 1.000 | 0.080 | 15 | 78552014 | 3 prime UTR variant | A/G;T | snv | 1 | |||
rs12901682 | 0.851 | 0.200 | 15 | 78540881 | 5 prime UTR variant | A/C;T | snv | 1 |