"GenomeConnect, ClinGen"[submitter] AND "LRBA"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 403049	NM_001364905.1(LRBA):c.7849+10A>G	LRBA	Single nucleotide variant (intron variant)	Combined immunodeficiency due to LRBA deficiency +2 more	GBenign
Select item 576122	NM_001364905.1(LRBA):c.4855G>T (p.Val1619Leu)	LRBA (V1619L)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 196133	NM_001364905.1(LRBA):c.4569+9C>T	LRBA	Single nucleotide variant (intron variant)	not specified +1 more	GBenign

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