Gene: PRPH2 ×
Source: UNIPROT ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs61755794
rs61755794
PRPH2
0.800 GeneticVariation UNIPROT

dbSNP: rs61754402
rs61754402
PRPH2
0.700 GeneticVariation UNIPROT

dbSNP: rs61755770
rs61755770
PRPH2
0.700 GeneticVariation UNIPROT

dbSNP: rs61755781
rs61755781
PRPH2
0.700 GeneticVariation UNIPROT

dbSNP: rs61755783
rs61755783
PRPH2
0.700 GeneticVariation UNIPROT

dbSNP: rs61755785
rs61755785
PRPH2
0.700 GeneticVariation UNIPROT

dbSNP: rs61755788
rs61755788
PRPH2
0.700 GeneticVariation UNIPROT

dbSNP: rs61755797
rs61755797
PRPH2
0.700 GeneticVariation UNIPROT

dbSNP: rs61755798
rs61755798
PRPH2
0.700 GeneticVariation UNIPROT

dbSNP: rs61755799
rs61755799
PRPH2
0.700 GeneticVariation UNIPROT

dbSNP: rs62645935
rs62645935
PRPH2
0.700 GeneticVariation UNIPROT

dbSNP: rs61755806
rs61755806
PRPH2
0.800 GeneticVariation UNIPROT Autosomal dominant retinitis pigmentosa: a novel mutation at the peripherin/RDS locus in the original 6p-linked pedigree. 1427912

1992
dbSNP: rs61755816
rs61755816
PRPH2
0.800 GeneticVariation UNIPROT Autosomal dominant retinitis pigmentosa: a novel mutation at the peripherin/RDS locus in the original 6p-linked pedigree. 1427912

1992
dbSNP: rs121918563
rs121918563
PRPH2
0.700 GeneticVariation UNIPROT Autosomal dominant retinitis pigmentosa: a novel mutation at the peripherin/RDS locus in the original 6p-linked pedigree. 1427912

1992
dbSNP: rs139185976
rs139185976
PRPH2
0.700 GeneticVariation UNIPROT Autosomal dominant retinitis pigmentosa: a novel mutation at the peripherin/RDS locus in the original 6p-linked pedigree. 1427912

1992
dbSNP: rs61755800
rs61755800
PRPH2
0.700 GeneticVariation UNIPROT Autosomal dominant retinitis pigmentosa: a novel mutation at the peripherin/RDS locus in the original 6p-linked pedigree. 1427912

1992
dbSNP: rs61755804
rs61755804
PRPH2
0.700 GeneticVariation UNIPROT Autosomal dominant retinitis pigmentosa: a novel mutation at the peripherin/RDS locus in the original 6p-linked pedigree. 1427912

1992
dbSNP: rs61755805
rs61755805
PRPH2
0.700 GeneticVariation UNIPROT Autosomal dominant retinitis pigmentosa: a novel mutation at the peripherin/RDS locus in the original 6p-linked pedigree. 1427912

1992
dbSNP: rs61755806
rs61755806
PRPH2
0.800 GeneticVariation UNIPROT Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa. 1684223

1991
dbSNP: rs61755816
rs61755816
PRPH2
0.800 GeneticVariation UNIPROT Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa. 1684223

1991
dbSNP: rs121918563
rs121918563
PRPH2
0.700 GeneticVariation UNIPROT Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa. 1684223

1991
dbSNP: rs139185976
rs139185976
PRPH2
0.700 GeneticVariation UNIPROT Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa. 1684223

1991
dbSNP: rs61755800
rs61755800
PRPH2
0.700 GeneticVariation UNIPROT Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa. 1684223

1991
dbSNP: rs61755804
rs61755804
PRPH2
0.700 GeneticVariation UNIPROT Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa. 1684223

1991
dbSNP: rs61755805
rs61755805
PRPH2
0.700 GeneticVariation UNIPROT Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa. 1684223

1991