FZD4, frizzled class receptor 4, 8322
N. diseases: 239; N. variants: 28
Source: ALL
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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.790 | 0.240 | 11 | 86952443 | missense variant | T/A;C | snv | 4.0E-06; 2.4E-05 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.800 | 1.000 | 13 | 2002 | 2010 | |||||||
|
1.000 | 0.080 | 11 | 86951751 | missense variant | C/G | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.800 | 1.000 | 13 | 2002 | 2010 | ||||||||
|
1.000 | 0.080 | 11 | 86951732 | missense variant | T/C | snv | 4.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.800 | 1.000 | 13 | 2002 | 2010 | |||||||
|
0.882 | 0.080 | 11 | 86951506 | missense variant | C/G;T | snv | 1.2E-05 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.800 | 1.000 | 13 | 2002 | 2010 | |||||||
|
0.925 | 0.080 | 11 | 86951990 | missense variant | T/C | snv | 5.1E-04 | 5.2E-04 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 1.000 | 13 | 2002 | 2010 | ||||||
|
1.000 | 0.080 | 11 | 86954968 | missense variant | C/G | snv | 2.9E-04 | 2.9E-04 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 1.000 | 13 | 2002 | 2010 | ||||||
|
0.882 | 0.080 | 11 | 86954989 | missense variant | G/A | snv | 1.7E-02 | 1.3E-02 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 1.000 | 13 | 2002 | 2010 | ||||||
|
1.000 | 0.080 | 11 | 86954979 | missense variant | C/T | snv | 7.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 1.000 | 13 | 2002 | 2010 | |||||||
|
0.925 | 0.080 | 11 | 86954881 | missense variant | G/A | snv | 5.2E-04 | 1.5E-04 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 1.000 | 13 | 2002 | 2010 | ||||||
|
1.000 | 0.080 | 11 | 86952442 | missense variant | A/G | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 1.000 | 13 | 2002 | 2010 | ||||||||
|
1.000 | 0.080 | 11 | 86952287 | missense variant | T/C | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 1.000 | 13 | 2002 | 2010 | ||||||||
|
0.925 | 0.080 | 11 | 86952215 | missense variant | A/G | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 1.000 | 13 | 2002 | 2010 | ||||||||
|
1.000 | 0.080 | 11 | 86952146 | missense variant | A/G | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 1.000 | 13 | 2002 | 2010 | ||||||||
|
1.000 | 0.080 | 11 | 86951423 | missense variant | T/G | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 1.000 | 13 | 2002 | 2010 | ||||||||
|
1.000 | 0.080 | 11 | 86951293 | missense variant | C/T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 1.000 | 13 | 2002 | 2010 | ||||||||
|
1.000 | 0.080 | 11 | 86951266 | missense variant | G/A;C | snv | 1.6E-05 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 1.000 | 13 | 2002 | 2010 | |||||||
|
1.000 | 0.080 | 11 | 86952145 | missense variant | C/T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 11 | 86951272 | inframe deletion | CCACAT/- | delins |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 11 | 86951254 | frameshift variant | AG/- | delins |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 0 |