RS201241191 FTL
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
sporadic abdominal aortic aneurysm
Neuroferritinopathy
Hereditary hyperferritinemia with congenital cataracts
FTL-related disorder
sporadic abdominal aortic aneurysm
Neuroferritinopathy
Hereditary hyperferritinemia with congenital cataracts
FTL-related disorder
Other Variants in FTL