Gene: BEST1 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267606676
rs267606676
BEST1 ; LOC107984334
A 0.700 CausalMutation CLINVAR Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy. 30718709

2019
dbSNP: rs1555099048
rs1555099048
BEST1 ; LOC107984334
G 0.700 GeneticVariation CLINVAR

dbSNP: rs372989281
rs372989281
BEST1 ; LOC107984334
T 0.700 CausalMutation CLINVAR