RS121918289 BEST1

Health Risk Chr 11:61955726
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal dominant vitreoretinochoroidopathy
Retinal dystrophy
Autosomal dominant vitreoretinochoroidopathy
Retinal dystrophy
Other Variants in BEST1
rs28940273 rs28940274 rs28941468 rs121918285 rs28941469 rs28940275 rs121918283 rs28940276 rs1805142 rs1800995
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