Source: UNIPROT ×
Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
---|---|---|---|---|---|---|---|---|---|---|
|
0.800 | GeneticVariation | UNIPROT | Rhodopsin mutation G90D and a molecular mechanism for congenital night blindness. | 8107847 | 1994 |
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|
0.800 | GeneticVariation | UNIPROT | Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness. | 8358437 | 1993 |
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|
0.800 | GeneticVariation | UNIPROT | Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutation. | 7846071 | 1995 |
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|
0.800 | GeneticVariation | UNIPROT | A novel mutation within the rhodopsin gene (Thr-94-Ile) causing autosomal dominant congenital stationary night blindness. | 9888392 | 1999 |
||||
|
0.800 | GeneticVariation | UNIPROT | A novel mutation within the rhodopsin gene (Thr-94-Ile) causing autosomal dominant congenital stationary night blindness. | 9888392 | 1999 |
||||
|
0.800 | GeneticVariation | UNIPROT | Rhodopsin mutation G90D and a molecular mechanism for congenital night blindness. | 8107847 | 1994 |
||||
|
0.800 | GeneticVariation | UNIPROT | Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness. | 8358437 | 1993 |
||||
|
0.800 | GeneticVariation | UNIPROT | Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutation. | 7846071 | 1995 |
||||
|
0.800 | GeneticVariation | UNIPROT | Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness. | 8358437 | 1993 |
||||
|
0.800 | GeneticVariation | UNIPROT | A novel mutation within the rhodopsin gene (Thr-94-Ile) causing autosomal dominant congenital stationary night blindness. | 9888392 | 1999 |
||||
|
0.800 | GeneticVariation | UNIPROT | Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutation. | 7846071 | 1995 |
||||
|
0.800 | GeneticVariation | UNIPROT | Rhodopsin mutation G90D and a molecular mechanism for congenital night blindness. | 8107847 | 1994 |