"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "LILRB3"[ge - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2650428	NM_006864.4(LILRB3):c.1096C>T (p.Leu366=)	LILRA6, LILRB3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2650429	NM_006864.4(LILRB3):c.1095A>G (p.Pro365=)	LILRB3, LILRA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2672793	GRCh37/hg19 19q13.42(chr19:54544215-54881884)x3	CNOT3, LAIR1 +18 more	Copy number gain	not provided	GUncertain significance

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