RS80338765 FBLN5
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What This Variant Does
"CLNSIG=5
Associated Conditions
Cutis laxa
autosomal recessive
type 1A
Macular degeneration
age-related
3
autosomal dominant
Cutis laxa
autosomal recessive
type 1A
Macular degeneration
age-related
3
autosomal dominant
Other Variants in FBLN5