Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
rs1057519903 | 0.683 | 0.080 | 1 | 226064434 | missense variant | A/T | snv | 28 | |||
rs1555535032 | 0.882 | 0.120 | 17 | 31338734 | frameshift variant | TTAC/- | delins | 9 | |||
rs727502902 | 0.882 | 0.080 | 7 | 140753338 | inframe insertion | -/TAG | delins | 4.0E-06 | 4 | ||
rs777345988 | 0.851 | 0.080 | 6 | 135203257 | missense variant | A/C;T | snv | 4.0E-06 | 4 | ||
rs9694676 | 0.925 | 0.080 | 8 | 104588948 | 5 prime UTR variant | A/G | snv | 8.6E-02 | 0.20 | 2 |