"GeneDx"[submitter] AND "LOC130060153"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59583	GRCh38/hg38 17p13.1(chr17:7478195-8435524)x1	ALOX12B, ALOX15B +191 more	Copy number loss	See cases	GPathogenic
Select item 1168780	NM_003809.3(TNFSF12):c.72C>T (p.Leu24=)	LOC130060153, TNFSF12 +1 more	Single nucleotide variant (synonymous variant +1 more)	Common variable immunodeficiency +1 more	GBenign