"Clinical Genetics, Academic Medical Center"[submitter] AND "LRIT3"[ge - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 900733	NM_198506.5(LRIT3):c.158C>T (p.Thr53Met)	LRIT3 (T53M)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 197395	NM_198506.5(LRIT3):c.1182A>G (p.Thr394=)	LRIT3	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 197396	NM_198506.5(LRIT3):c.1621A>G (p.Ile541Val)	LRIT3 (I541V)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign

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