Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs147346345
rs147346345
A 0.710 GeneticVariation CLINVAR Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy. 30718709

2019

dbSNP: rs756678484
rs756678484
A 0.700 CausalMutation CLINVAR Biallelic mutation of protocadherin-21 (PCDH21) causes retinal degeneration in humans. 20087419

2010

dbSNP: rs1554857529
rs1554857529
G 0.700 GeneticVariation CLINVAR

dbSNP: rs878853347
rs878853347
TC 0.700 GeneticVariation CLINVAR