RS760738833 FSCN2

Health Risk Chr 17:81537016
Upload your DNA to see your genotype for this variant.
Associated Conditions
Retinal dystrophy
Retinal dystrophy
Other Variants in FSCN2
rs376633374 rs182593453 rs370156011 rs769242340 rs181420326 rs368687488 rs201054437 rs370382419 rs181961770 rs1048819854
Ask Dr. Hemsworth about this variant