RS753614067 BEST1;FTH1

Health Risk Chr 11:61955870
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive bestrophinopathy
Retinal dystrophy
Autosomal recessive bestrophinopathy
Retinal dystrophy
Other Variants in BEST1;FTH1
rs200277476 rs1805143 rs1801327 rs775979290 rs1941820458 rs750906488
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