Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894867
rs104894867
0.800 GeneticVariation UNIPROT Overview of the mutation spectrum in familial exudative vitreoretinopathy and Norrie disease with identification of 21 novel variants in FZD4, LRP5, and NDP. 20340138

2010

dbSNP: rs104894868
rs104894868
0.800 GeneticVariation UNIPROT Overview of the mutation spectrum in familial exudative vitreoretinopathy and Norrie disease with identification of 21 novel variants in FZD4, LRP5, and NDP. 20340138

2010

dbSNP: rs104894869
rs104894869
0.800 GeneticVariation UNIPROT Overview of the mutation spectrum in familial exudative vitreoretinopathy and Norrie disease with identification of 21 novel variants in FZD4, LRP5, and NDP. 20340138

2010

dbSNP: rs104894870
rs104894870
0.800 GeneticVariation UNIPROT Overview of the mutation spectrum in familial exudative vitreoretinopathy and Norrie disease with identification of 21 novel variants in FZD4, LRP5, and NDP. 20340138

2010

dbSNP: rs104894871
rs104894871
0.800 GeneticVariation UNIPROT Overview of the mutation spectrum in familial exudative vitreoretinopathy and Norrie disease with identification of 21 novel variants in FZD4, LRP5, and NDP. 20340138

2010

dbSNP: rs104894872
rs104894872
0.800 GeneticVariation UNIPROT Overview of the mutation spectrum in familial exudative vitreoretinopathy and Norrie disease with identification of 21 novel variants in FZD4, LRP5, and NDP. 20340138

2010

dbSNP: rs104894875
rs104894875
0.800 GeneticVariation UNIPROT Overview of the mutation spectrum in familial exudative vitreoretinopathy and Norrie disease with identification of 21 novel variants in FZD4, LRP5, and NDP. 20340138

2010

dbSNP: rs104894877
rs104894877
0.800 GeneticVariation UNIPROT Overview of the mutation spectrum in familial exudative vitreoretinopathy and Norrie disease with identification of 21 novel variants in FZD4, LRP5, and NDP. 20340138

2010

dbSNP: rs104894879
rs104894879
0.800 GeneticVariation UNIPROT Overview of the mutation spectrum in familial exudative vitreoretinopathy and Norrie disease with identification of 21 novel variants in FZD4, LRP5, and NDP. 20340138

2010

dbSNP: rs104894880
rs104894880
0.800 GeneticVariation UNIPROT Overview of the mutation spectrum in familial exudative vitreoretinopathy and Norrie disease with identification of 21 novel variants in FZD4, LRP5, and NDP. 20340138

2010

dbSNP: rs104894883
rs104894883
0.800 GeneticVariation UNIPROT Overview of the mutation spectrum in familial exudative vitreoretinopathy and Norrie disease with identification of 21 novel variants in FZD4, LRP5, and NDP. 20340138

2010

dbSNP: rs104894867
rs104894867
0.800 GeneticVariation UNIPROT Novel mutations in Norrie disease gene in Japanese patients with Norrie disease and familial exudative vitreoretinopathy. 17325173

2007

dbSNP: rs104894867
rs104894867
0.800 GeneticVariation UNIPROT Retinal phenotype-genotype correlation of pediatric patients expressing mutations in the Norrie disease gene. 17296899

2007

dbSNP: rs104894867
rs104894867
0.800 GeneticVariation UNIPROT A novel missense mutation in the NDP gene in a child with Norrie disease and severe neurological involvement including infantile spasms. 17334993

2007

dbSNP: rs104894868
rs104894868
0.800 GeneticVariation UNIPROT A novel missense mutation in the NDP gene in a child with Norrie disease and severe neurological involvement including infantile spasms. 17334993

2007

dbSNP: rs104894868
rs104894868
0.800 GeneticVariation UNIPROT Retinal phenotype-genotype correlation of pediatric patients expressing mutations in the Norrie disease gene. 17296899

2007

dbSNP: rs104894868
rs104894868
0.800 GeneticVariation UNIPROT Novel mutations in Norrie disease gene in Japanese patients with Norrie disease and familial exudative vitreoretinopathy. 17325173

2007

dbSNP: rs104894869
rs104894869
0.800 GeneticVariation UNIPROT Novel mutations in Norrie disease gene in Japanese patients with Norrie disease and familial exudative vitreoretinopathy. 17325173

2007

dbSNP: rs104894869
rs104894869
0.800 GeneticVariation UNIPROT Retinal phenotype-genotype correlation of pediatric patients expressing mutations in the Norrie disease gene. 17296899

2007

dbSNP: rs104894869
rs104894869
0.800 GeneticVariation UNIPROT A novel missense mutation in the NDP gene in a child with Norrie disease and severe neurological involvement including infantile spasms. 17334993

2007

dbSNP: rs104894870
rs104894870
0.800 GeneticVariation UNIPROT A novel missense mutation in the NDP gene in a child with Norrie disease and severe neurological involvement including infantile spasms. 17334993

2007

dbSNP: rs104894870
rs104894870
0.800 GeneticVariation UNIPROT Novel mutations in Norrie disease gene in Japanese patients with Norrie disease and familial exudative vitreoretinopathy. 17325173

2007

dbSNP: rs104894870
rs104894870
0.800 GeneticVariation UNIPROT Retinal phenotype-genotype correlation of pediatric patients expressing mutations in the Norrie disease gene. 17296899

2007

dbSNP: rs104894871
rs104894871
0.800 GeneticVariation UNIPROT Novel mutations in Norrie disease gene in Japanese patients with Norrie disease and familial exudative vitreoretinopathy. 17325173

2007

dbSNP: rs104894871
rs104894871
0.800 GeneticVariation UNIPROT Retinal phenotype-genotype correlation of pediatric patients expressing mutations in the Norrie disease gene. 17296899

2007