Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs62645944
rs62645944
ABCA4
A 0.710 GeneticVariation CLINVAR Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy. 30718709

2019
dbSNP: rs62645944
rs62645944
ABCA4
0.710 GeneticVariation BEFREE Another patient in this family with a severe type of retinitis pigmentosa (RP) carried the 768G-->T mutation homozygously. 15019334

2004