Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267607139
rs267607139
TRPM1
0.800 GeneticVariation UNIPROT Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans. 19878917

2009
dbSNP: rs267607139
rs267607139
TRPM1
0.800 GeneticVariation UNIPROT TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness. 19896113

2009
dbSNP: rs267607139
rs267607139
TRPM1
0.800 GeneticVariation UNIPROT Mutations in TRPM1 are a common cause of complete congenital stationary night blindness. 19896109

2009
dbSNP: rs267607139
rs267607139
TRPM1
T 0.800 CausalMutation CLINVAR