"GeneDx"[submitter] AND "LOC129994951"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59672	GRCh38/hg38 5q21.3-33.2(chr5:106619588-156124387)x1	ABLIM3, ACSL6 +1672 more	Copy number loss	See cases	GPathogenic
Select item 1235095	NC_000005.10:g.148826364G>C	ADRB2, LOC129994951	Single nucleotide variant	not provided	GBenign
Select item 1264990	NC_000005.10:g.148826426C>T	ADRB2, LOC129994951	Single nucleotide variant	not provided	GBenign
Select item 1259578	NC_000005.10:g.148826465C>T	ADRB2, LOC129994951	Single nucleotide variant	not provided	GBenign

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