"GeneDx"[submitter] AND "RPS28"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59082	GRCh38/hg38 19p13.3-13.2(chr19:1972245-9648879)x3	LOC130063254, LOC130063255 +810 more	Copy number gain	See cases	GPathogenic
Select item 1224045	NC_000019.10:g.8321172G>C	NDUFA7, RPS28	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1265048	NC_000019.10:g.8321175T>G	RPS28, NDUFA7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1276445	NC_000019.10:g.8321422G>A	RPS28	Single nucleotide variant	not provided	GBenign
Select item 1257584	NC_000019.10:g.8321483C>T	RPS28	Single nucleotide variant	not provided	GBenign
Select item 668538	NM_001031.5(RPS28):c.87+6C>T	RPS28	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1268375	NM_001031.5(RPS28):c.87+75T>C	RPS28	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1181154	NM_001031.5(RPS28):c.87+114G>A	RPS28	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1244664	NM_001031.5(RPS28):c.*16+23T>C	RPS28	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1252932	NM_001031.5(RPS28):c.*68G>A	RPS28	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign