Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs41293497 | 0.724 | 0.440 | 13 | 32340037 | stop gained | C/A;G;T | snv | 4.0E-06; 2.0E-05 | 14 | ||
rs80358807 | 0.763 | 0.280 | 13 | 32340146 | stop gained | C/T | snv | 10 | |||
rs28897743 | 0.827 | 0.280 | 13 | 32346896 | missense variant | G/A;C;T | snv | 4.0E-06 | 8 | ||
rs397507758 | 0.807 | 0.200 | 13 | 32339456 | stop gained | C/T | snv | 6 | |||
rs80359306 | 0.827 | 0.280 | 13 | 32333284 | frameshift variant | A/-;AA | delins | 6 | |||
rs28897759 | 0.851 | 0.200 | 13 | 32394803 | missense variant | A/G;T | snv | 4.0E-06; 4.0E-06 | 5 | ||
rs41293477 | 0.851 | 0.200 | 13 | 32337513 | stop gained | T/G | snv | 7.0E-06 | 5 | ||
rs80358547 | 0.851 | 0.200 | 13 | 32316462 | start lost | T/A;C;G | snv | 8.0E-06 | 5 | ||
rs80358561 | 0.851 | 0.200 | 13 | 32319323 | stop gained | T/G | snv | 5 | |||
rs80359152 | 0.851 | 0.200 | 13 | 32379800 | missense variant | G/A | snv | 5 | |||
rs80359770 | 0.851 | 0.200 | 13 | 32332429 | frameshift variant | A/-;AA | delins | 5 | |||
rs483353122 | 0.851 | 0.200 | 13 | 32363410 | frameshift variant | -/AG | ins | 4 | |||
rs80358702 | 0.882 | 0.080 | 13 | 32326150 | missense variant | G/A;C | snv | 4 | |||
rs80359011 | 0.882 | 0.200 | 13 | 32362574 | stop gained | G/A;C | snv | 4 | |||
rs80359598 | 0.882 | 0.200 | 13 | 32340837 | frameshift variant | ACAA/- | delins | 4 | |||
rs886040340 | 0.882 | 0.080 | 13 | 32319111 | frameshift variant | -/C | delins | 4 | |||
rs80359379 | 0.882 | 0.080 | 13 | 32337615 | frameshift variant | CC/-;C;CCC | delins | 3 | |||
rs1555283031 | 0.925 | 0.080 | 13 | 32337423 | frameshift variant | ACAT/- | del | 2 | |||
rs397507990 | 0.925 | 0.080 | 13 | 32370999 | frameshift variant | AA/-;AAA | delins | 2 |