C1833213[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 16480	NM_000146.4(FTL):c.-161C>T	FTL	Single nucleotide variant (5 prime UTR variant)	Hereditary hyperferritinemia with congenital cataracts +2 more	GPathogenic/Likely pathogenic
Select item 16482	NM_000146.4(FTL):c.-149G>C	FTL	Single nucleotide variant (5 prime UTR variant)	Neuroferritinopathy +2 more	GLikely pathogenic