RS144288844 FBLN5
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What This Variant Does
"CLNSIG=5
Associated Conditions
Macular degeneration
age-related
3
Cutis laxa
autosomal recessive
type 1A
autosomal dominant 2
Charcot-Marie-Tooth disease
demyelinating
IIA 1H
Hereditary sensorimotor neuropathy with hyperelastic skin
Retinal dystrophy
Optic atrophy
Macular degeneration
age-related
Other Variants in FBLN5