Variant | Gene | N. diseases v | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
11 | 0.807 | 0.200 | 1 | 26767868 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
6 | 0.827 | 0.280 | 20 | 45304356 | missense variant | C/G | snv | 0.700 | 0 | ||||||||
|
3 | 0.882 | 0.160 | 18 | 3457498 | missense variant | T/C | snv | 2.6E-04 | 1.1E-04 | 0.010 | 1.000 | 1 | 2006 | 2006 | |||
|
3 | 0.882 | 0.160 | 20 | 38148005 | missense variant | G/A;C;T | snv | 1.6E-05; 4.1E-06 | 0.010 | 1.000 | 1 | 2002 | 2002 | ||||
|
4 | 0.882 | 0.160 | 7 | 155806509 | missense variant | A/C;G | snv | 0.700 | 0 | ||||||||
|
3 | 0.882 | 0.160 | 10 | 101771522 | stop gained | G/A | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
2 | 0.925 | 0.120 | 18 | 3456525 | missense variant | C/G | snv | 0.010 | 1.000 | 1 | 2007 | 2007 | |||||
|
2 | 0.925 | 0.120 | 18 | 3457392 | missense variant | C/T | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2002 | 2002 | ||||
|
2 | 0.925 | 0.120 | 7 | 155811823 | missense variant | C/G | snv | 0.710 | 1.000 | 1 | 2005 | 2005 | |||||
|
2 | 0.925 | 0.120 | 7 | 155806296 | missense variant | C/G | snv | 0.710 | 1.000 | 1 | 2005 | 2005 | |||||
|
2 | 0.925 | 0.120 | 7 | 155803618 | missense variant | A/T | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.120 | 7 | 155803613 | missense variant | C/T | snv | 4.4E-05 | 5.6E-05 | 0.700 | 0 | ||||||
|
2 | 0.925 | 0.120 | 7 | 155811825 | stop gained | G/A | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.120 | 7 | 155806545 | stop gained | T/A | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.120 | 7 | 155803439 | stop gained | C/A;T | snv | 1.5E-05 | 0.700 | 0 | |||||||
|
2 | 0.925 | 0.120 | 7 | 155803019 | missense variant | G/C;T | snv | 3.7E-05 | 0.700 | 0 | |||||||
|
2 | 0.925 | 0.120 | 7 | 155811860 | missense variant | T/A | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.120 | 7 | 155803523 | stop gained | C/A;G | snv | 1.5E-05 | 0.700 | 0 | |||||||
|
2 | 0.925 | 0.120 | 7 | 155806513 | missense variant | G/A;T | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
2 | 0.925 | 0.120 | 7 | 155812032 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.120 | 13 | 99985400 | frameshift variant | -/C | delins | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.120 | 13 | 99983104 | frameshift variant | GAGAACC/- | delins | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.120 | 7 | 155803481 | inframe deletion | GCGGCGGTGAGCAGCAGGCGC/- | delins | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.120 | 7 | 155803149 | inframe deletion | GCGCGAAGG/- | delins | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.120 | 7 | 155803625 | missense variant | C/T | snv | 7.0E-06 | 0.700 | 0 |