Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4807542 | 1.000 | 0.120 | 19 | 1104079 | synonymous variant | G/A;C | snv | 0.22; 1.8E-05 | 3 | ||
rs8046011 | 1.000 | 0.120 | 16 | 11226805 | downstream gene variant | G/A;T | snv | 3 | |||
rs2427827 | 1.000 | 0.120 | 1 | 159302021 | intron variant | T/C | snv | 0.65 | 2 | ||
rs62408225 | 1.000 | 0.120 | 6 | 90246690 | intron variant | A/G | snv | 0.26 | 2 | ||
rs113795008 | 1.000 | 0.120 | 11 | 192836 | intron variant | A/G | snv | 0.17 | 1 | ||
rs17718444 | 1.000 | 0.120 | 3 | 71450250 | intron variant | C/T | snv | 0.27 | 1 | ||
rs2280540 | 1.000 | 0.120 | 11 | 192997 | intron variant | G/A;C;T | snv | 1 | |||
rs338598 | 1.000 | 0.120 | 19 | 41195623 | intron variant | C/A;G;T | snv | 1 | |||
rs6543124 | 1.000 | 0.120 | 2 | 102370999 | intron variant | T/A | snv | 0.44 | 1 |