Related gene-specific medical variations for Gene (Select 3683) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3111346	NM_002209.3(ITGAL):c.1930A>C (p.Met644Leu)	ITGAL, ITGAL-AS1 (M561L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302656	NM_002209.3(ITGAL):c.1970A>C (p.Lys657Thr)	ITGAL, ITGAL-AS1 (K574T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219484	NM_002209.3(ITGAL):c.1954A>G (p.Ile652Val)	ITGAL, ITGAL-AS1 (I569V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign

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