LOC126057115[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 151481	GRCh37/hg19 19q13.42(chr19:54769799-54835745)x3	LILRA3, LILRA5 +6 more	Copy number gain	See cases	GBenign
Select item 151454	GRCh37/hg19 19q13.42(chr19:54769799-54864136)x3	LOC126862931, LAIR1 +10 more	Copy number gain	See cases	GLikely benign
Select item 2241971	NM_006865.5(LILRA3):c.59A>G (p.His20Arg)	LILRA3, LOC126057115 (H20R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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