Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
---|---|---|---|---|---|---|---|---|---|---|
|
0.800 | GeneticVariation | UNIPROT | |||||||
|
0.700 | GeneticVariation | UNIPROT | |||||||
|
0.700 | GeneticVariation | UNIPROT | |||||||
|
0.700 | GeneticVariation | UNIPROT | |||||||
|
0.700 | GeneticVariation | UNIPROT | |||||||
|
0.700 | GeneticVariation | UNIPROT | |||||||
|
0.700 | GeneticVariation | UNIPROT | |||||||
|
0.700 | GeneticVariation | UNIPROT | |||||||
|
0.700 | GeneticVariation | UNIPROT | |||||||
|
0.700 | GeneticVariation | UNIPROT | |||||||
|
0.700 | GeneticVariation | UNIPROT | |||||||
|
0.800 | GeneticVariation | UNIPROT | A three-base-pair deletion in the peripherin-RDS gene in one form of retinitis pigmentosa. | 1749427 | 1991 |
||||
|
0.800 | GeneticVariation | UNIPROT | Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa. | 1684223 | 1991 |
||||
|
0.800 | GeneticVariation | UNIPROT | Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa. | 1684223 | 1991 |
||||
|
0.800 | GeneticVariation | UNIPROT | A three-base-pair deletion in the peripherin-RDS gene in one form of retinitis pigmentosa. | 1749427 | 1991 |
||||
|
0.700 | GeneticVariation | UNIPROT | A three-base-pair deletion in the peripherin-RDS gene in one form of retinitis pigmentosa. | 1749427 | 1991 |
||||
|
0.700 | GeneticVariation | UNIPROT | Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa. | 1684223 | 1991 |
||||
|
0.700 | GeneticVariation | UNIPROT | A three-base-pair deletion in the peripherin-RDS gene in one form of retinitis pigmentosa. | 1749427 | 1991 |
||||
|
0.700 | GeneticVariation | UNIPROT | Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa. | 1684223 | 1991 |
||||
|
0.700 | GeneticVariation | UNIPROT | Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa. | 1684223 | 1991 |
||||
|
0.700 | GeneticVariation | UNIPROT | A three-base-pair deletion in the peripherin-RDS gene in one form of retinitis pigmentosa. | 1749427 | 1991 |
||||
|
0.700 | GeneticVariation | UNIPROT | A three-base-pair deletion in the peripherin-RDS gene in one form of retinitis pigmentosa. | 1749427 | 1991 |
||||
|
0.700 | GeneticVariation | UNIPROT | Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa. | 1684223 | 1991 |
||||
|
0.700 | GeneticVariation | UNIPROT | A three-base-pair deletion in the peripherin-RDS gene in one form of retinitis pigmentosa. | 1749427 | 1991 |
||||
|
0.700 | GeneticVariation | UNIPROT | Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa. | 1684223 | 1991 |