Variant | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Disease Class | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.827 | 0.120 | 6 | 42721781 | missense variant | A/G | snv | 8.0E-06 | 1.4E-05 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 1.000 | 11 | 1991 | 2016 | ||||||
|
0.827 | 0.120 | 6 | 42721781 | missense variant | A/G | snv | 8.0E-06 | 1.4E-05 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.010 | 1.000 | 1 | 2001 | 2001 | ||||||
|
0.827 | 0.120 | 6 | 42721781 | missense variant | A/G | snv | 8.0E-06 | 1.4E-05 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 1997 | 1997 | ||||||
|
0.827 | 0.120 | 6 | 42721781 | missense variant | A/G | snv | 8.0E-06 | 1.4E-05 |
|
0.700 | 0 | ||||||||||
|
0.827 | 0.120 | 6 | 42721781 | missense variant | A/G | snv | 8.0E-06 | 1.4E-05 |
|
Eye Diseases | 0.700 | 0 | |||||||||
|
0.827 | 0.120 | 6 | 42721781 | missense variant | A/G | snv | 8.0E-06 | 1.4E-05 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 0 | |||||||||
|
1.000 | 0.080 | 6 | 42704419 | stop gained | G/T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.710 | 1.000 | 1 | 1997 | 1997 | ||||||||
|
1.000 | 0.080 | 6 | 42722333 | start lost | A/G | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 6 | 42698389 | stop gained | C/T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 0 | |||||||||||
|
0.807 | 0.080 | 6 | 42704609 | missense variant | C/A;T | snv | 4.0E-06 |
|
Eye Diseases | 0.800 | 1.000 | 4 | 2006 | 2016 | |||||||
|
0.807 | 0.080 | 6 | 42704609 | missense variant | C/A;T | snv | 4.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 1.000 | 3 | 2003 | 2012 | |||||||
|
0.807 | 0.080 | 6 | 42704609 | missense variant | C/A;T | snv | 4.0E-06 |
|
Eye Diseases | 0.020 | 1.000 | 2 | 2006 | 2011 | |||||||
|
0.807 | 0.080 | 6 | 42704609 | missense variant | C/A;T | snv | 4.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||||
|
0.807 | 0.080 | 6 | 42704609 | missense variant | C/A;T | snv | 4.0E-06 |
|
Eye Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.807 | 0.080 | 6 | 42704609 | missense variant | C/A;T | snv | 4.0E-06 |
|
Eye Diseases | 0.700 | 0 | ||||||||||
|
0.882 | 0.080 | 6 | 42704570 | missense variant | C/T | snv | 4.8E-05 | 9.8E-05 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 1.000 | 11 | 1991 | 2016 | ||||||
|
0.882 | 0.080 | 6 | 42704570 | missense variant | C/T | snv | 4.8E-05 | 9.8E-05 |
|
Eye Diseases | 0.700 | 1.000 | 2 | 1997 | 2019 | ||||||
|
0.882 | 0.080 | 6 | 42704570 | missense variant | C/T | snv | 4.8E-05 | 9.8E-05 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.010 | 1.000 | 1 | 1998 | 1998 | ||||||
|
1.000 | 0.080 | 6 | 42698469 | frameshift variant | CGACGTCT/- | del |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 6 | 42704529 | missense variant | A/G | snv |
|
Eye Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 6 | 42704529 | missense variant | A/G | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 6 | 42704557 | missense variant | G/C | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 6 | 42704581 | stop gained | G/C | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 0 | |||||||||||
|
6 | 42722069 | frameshift variant | GCTGGGTC/- | del |
|
Eye Diseases | 0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||||
|
1.000 | 0.080 | 6 | 42722018 | frameshift variant | CA/- | delins |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 0 |