"LECT2-related disorder"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3042925	NM_002302.3(LECT2):c.432G>A (p.Ser144=)	LECT2	Single nucleotide variant (synonymous variant)	LECT2-related disorder	GLikely benign
Select item 3060729	NM_002302.3(LECT2):c.172A>G (p.Ile58Val)	LECT2 (I58V)	Single nucleotide variant (missense variant)	LECT2-related disorder	GBenign