RS200277476 BEST1;FTH1
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What This Variant Does
"CLNSIG=4
Associated Conditions
Autosomal recessive bestrophinopathy
Retinal dystrophy
Vitelliform macular dystrophy 2
Autosomal dominant vitreoretinochoroidopathy
Retinitis pigmentosa 50
Gastric cancer
Ovarian serous cystadenocarcinoma
Malignant tumor of esophagus
Nonpapillary renal cell carcinoma
BEST1-related dominant retinopathy
BEST1-related disorder
Incidental Discovery
Autosomal recessive bestrophinopathy
Retinal dystrophy
Vitelliform macular dystrophy 2
Other Variants in BEST1;FTH1