Gene: RHO ×
Source: UNIPROT ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893789
rs104893789
RHO
0.800 GeneticVariation UNIPROT A novel mutation within the rhodopsin gene (Thr-94-Ile) causing autosomal dominant congenital stationary night blindness. 9888392

1999
dbSNP: rs104893790
rs104893790
RHO
0.800 GeneticVariation UNIPROT A novel mutation within the rhodopsin gene (Thr-94-Ile) causing autosomal dominant congenital stationary night blindness. 9888392

1999
dbSNP: rs104893796
rs104893796
RHO
0.800 GeneticVariation UNIPROT A novel mutation within the rhodopsin gene (Thr-94-Ile) causing autosomal dominant congenital stationary night blindness. 9888392

1999
dbSNP: rs104893789
rs104893789
RHO
0.800 GeneticVariation UNIPROT Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutation. 7846071

1995
dbSNP: rs104893790
rs104893790
RHO
0.800 GeneticVariation UNIPROT Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutation. 7846071

1995
dbSNP: rs104893796
rs104893796
RHO
0.800 GeneticVariation UNIPROT Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutation. 7846071

1995
dbSNP: rs104893789
rs104893789
RHO
0.800 GeneticVariation UNIPROT Rhodopsin mutation G90D and a molecular mechanism for congenital night blindness. 8107847

1994
dbSNP: rs104893790
rs104893790
RHO
0.800 GeneticVariation UNIPROT Rhodopsin mutation G90D and a molecular mechanism for congenital night blindness. 8107847

1994
dbSNP: rs104893796
rs104893796
RHO
0.800 GeneticVariation UNIPROT Rhodopsin mutation G90D and a molecular mechanism for congenital night blindness. 8107847

1994
dbSNP: rs104893789
rs104893789
RHO
0.800 GeneticVariation UNIPROT Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness. 8358437

1993
dbSNP: rs104893790
rs104893790
RHO
0.800 GeneticVariation UNIPROT Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness. 8358437

1993
dbSNP: rs104893796
rs104893796
RHO
0.800 GeneticVariation UNIPROT Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness. 8358437

1993