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

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3057520	NM_001136472.2(LITAF):c.378-17TC[6]	LITAF	Microsatellite (intron variant)	LITAF-related disorder	GLikely benign
Select item 677273	NM_001136472.2(LITAF):c.377+1763A>G	LITAF (S138G)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 677272	NM_001136472.2(LITAF):c.377+1760C>T	LITAF (R137C)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign

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