Gene: NYX ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs62637034
rs62637034
NYX
0.700 GeneticVariation UNIPROT The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein. 11062472

2000
dbSNP: rs62637035
rs62637035
NYX
0.700 GeneticVariation UNIPROT The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein. 11062472

2000
dbSNP: rs62637035
rs62637035
NYX
0.700 GeneticVariation UNIPROT Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness. 11062471

2000
dbSNP: rs62637036
rs62637036
NYX
0.700 GeneticVariation UNIPROT Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness. 11062471

2000
dbSNP: rs62637036
rs62637036
NYX
0.700 GeneticVariation UNIPROT The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein. 11062472

2000
dbSNP: rs62637037
rs62637037
NYX
A 0.700 CausalMutation CLINVAR

dbSNP: rs62637038
rs62637038
NYX
0.700 GeneticVariation UNIPROT Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness. 11062471

2000
dbSNP: rs62637038
rs62637038
NYX
0.700 GeneticVariation UNIPROT The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein. 11062472

2000