RS759410076 BEST1
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Associated Conditions
Vitelliform macular dystrophy 2
Autosomal dominant vitreoretinochoroidopathy
Severe early-childhood-onset retinal dystrophy
Vitelliform macular dystrophy 2
Autosomal dominant vitreoretinochoroidopathy
Severe early-childhood-onset retinal dystrophy
Other Variants in BEST1