Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121918284
rs121918284
BEST1 ; LOC107984334
0.010 GeneticVariation BEFREE The p.R141H mutation is frequently seen together with multifocal vitelliform retinopathy and biallelic mutations in BEST1. 21192766

2011