RS376633374 FSCN2

Health Risk Chr 17:81528603
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Retinitis pigmentosa 30
Leber congenital amaurosis
Macular degeneration
Retinal dystrophy
Retinitis pigmentosa 30
Leber congenital amaurosis
Macular degeneration
Retinal dystrophy
Other Variants in FSCN2
rs182593453 rs370156011 rs769242340 rs181420326 rs368687488 rs201054437 rs370382419 rs181961770 rs1048819854 rs782414995
Ask Dr. Hemsworth about this variant