RS199869995 FTL

Health Risk Chr 19:48966341
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What This Variant Does
"CLNSIG=5
Associated Conditions
L-FERRITIN DEFICIENCY
AUTOSOMAL RECESSIVE
Inborn genetic diseases
L-FERRITIN DEFICIENCY
AUTOSOMAL RECESSIVE
Inborn genetic diseases
Other Variants in FTL
rs398124633 rs398124634 rs398124635 rs1555796939 rs398124636 rs398124637 rs398124638 rs398124639 rs104894685 rs1114167274
Ask Dr. Hemsworth about this variant