Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1800734 | 0.653 | 0.400 | 3 | 36993455 | 5 prime UTR variant | G/A | snv | 0.22 | 30 | ||
rs63750206 | 0.807 | 0.200 | 3 | 36996701 | missense variant | G/A;C;T | snv | 9 | |||
rs63751012 | 0.851 | 0.200 | 3 | 36993656 | stop gained | G/A;C;T | snv | 5 | |||
rs587779021 | 0.851 | 0.200 | 3 | 37008905 | missense variant | G/A;C | snv | 4 | |||
rs63750691 | 0.882 | 0.160 | 3 | 37017521 | stop gained | C/G | snv | 4 | |||
rs1434898623 | 1.000 | 0.080 | 3 | 37040295 | splice donor variant | G/A | snv | 3 | |||
rs63751701 | 0.925 | 0.080 | 3 | 36993663 | stop gained | G/A;T | snv | 3 | |||
rs1553651073 | 0.925 | 0.160 | 3 | 37025834 | frameshift variant | CA/- | delins | 2 | |||
rs587779018 | 0.925 | 0.160 | 3 | 37008855 | frameshift variant | T/-;TT | delins | 2 | |||
rs876658198 | 0.925 | 0.080 | 3 | 37028855 | missense variant | G/A | snv | 2 | |||
rs1114167435 | 1.000 | 0.080 | 3 | 37025932 | frameshift variant | AG/- | delins | 1 | |||
rs63750547 | 0.925 | 0.160 | 3 | 37020312 | stop gained | T/C;G | snv | 4.0E-06 | 3 | ||
rs876658657 | 0.677 | 0.280 | 3 | 37020356 | missense variant | A/G | snv | 4.0E-06 | 25 | ||
rs63750781 | 0.851 | 0.160 | 3 | 37004444 | missense variant | C/G;T | snv | 4.0E-06 | 6 | ||
rs779795819 | 0.925 | 0.080 | 3 | 37048526 | frameshift variant | -/ATTG | delins | 4.0E-06 | 2 | ||
rs1418586322 | 0.827 | 0.160 | 3 | 37050495 | missense variant | C/G | snv | 4.0E-06 | 6 | ||
rs1799977 | 0.662 | 0.440 | 3 | 37012077 | missense variant | A/C;G;T | snv | 0.23 | 28 |