"Illumina Laboratory Services, Illumina"[submitter] AND "NRROS"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1328539	NM_198565.3(NRROS):c.1222A>C (p.Asn408His)	NRROS (N408H)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2671619	Single allele	ABCC5, ABCF3 +145 more	Duplication	not provided	GPathogenic
Select item 2671595	Single allele	AADAC, AADACL2 +286 more	Duplication	not provided	GPathogenic
Select item 1328450	GRCh37/hg19 3q28-29(chr3:191866466-197842171)x1	ACAP2, APOD +48 more	Copy number loss	not provided	GPathogenic

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