"GeneDx"[submitter] AND "LOC129936439"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 57769	GRCh38/hg38 3p22.3-22.2(chr3:32322382-36775606)x1	ARPP21, ARPP21-AS1 +87 more	Copy number loss	See cases	GPathogenic
Select item 674864	NM_006371.5(CRTAP):c.1152+36C>A	CRTAP, LOC129936439	Single nucleotide variant (intron variant)	Osteogenesis imperfecta type 7 +1 more	GBenign
Select item 675028	NM_006371.5(CRTAP):c.1152+97A>G	CRTAP, LOC129936439	Single nucleotide variant (intron variant)	not provided	GBenign

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