RS397514540 FTL

Health Risk Chr 19:48965596
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary hyperferritinemia with congenital cataracts
Neuroferritinopathy
Hereditary hyperferritinemia with congenital cataracts
Neuroferritinopathy
Other Variants in FTL
rs398124633 rs398124634 rs398124635 rs1555796939 rs398124636 rs398124637 rs398124638 rs398124639 rs104894685 rs1114167274
Ask Dr. Hemsworth about this variant