"GeneDx"[submitter] AND "RPS27"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 60011	GRCh38/hg38 1q21.3(chr1:153759563-154219803)x1	C1orf43, CFAP141 +35 more	Copy number loss	See cases	GPathogenic
Select item 1286485	NM_001030.6(RPS27):c.115+109C>T	LOC126805872, RPS27	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1237561	NM_001030.6(RPS27):c.227-144_227-143insAA	RPS27	Insertion (intron variant)	not provided	GBenign
Select item 1222697	NC_000001.11:g.153992376dup	RPS27	Duplication	not provided	GBenign

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