Gene: CNGB3 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397515360
rs397515360
CNGB3
A 0.700 CausalMutation CLINVAR Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy. 30718709

2019
dbSNP: rs397515360
rs397515360
CNGB3
A 0.700 CausalMutation CLINVAR Genetic basis of total colourblindness among the Pingelapese islanders. 10888875

2000
dbSNP: rs775796581
rs775796581
CNGB3
T 0.700 CausalMutation CLINVAR Genetic basis of total colourblindness among the Pingelapese islanders. 10888875

2000
dbSNP: rs773372519
rs773372519
CNGB3
C 0.700 CausalMutation CLINVAR