"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC130006 - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 378086	NM_001144869.3(LIPT2):c.158C>T (p.Ala53Val)	LIPT2, LIPT2-AS1 +1 more (A53V)	Single nucleotide variant (missense variant)	LIPT2-related disorder +1 more	GBenign
Select item 3058612	NM_001144869.3(LIPT2):c.115C>T (p.Pro39Ser)	LIPT2, LIPT2-AS1 +1 more (P39S)	Single nucleotide variant (non-coding transcript variant +1 more)	LIPT2-related disorder	GLikely benign