Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs781463257
rs781463257
GRM6
A 0.700 CausalMutation CLINVAR A phenotypic study of congenital stationary night blindness (CSNB) associated with mutations in the GRM6 gene. 22008250

2012