List of variants in gene RPS28 reported as benign

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001031.5(RPS28):c.*68G>A	rs1057232	0.59529
NM_001031.5(RPS28):c.87+114G>A	rs2241590	0.45173
NM_001031.5(RPS28):c.*16+23T>C	rs4147644	0.26518
NC_000019.10:g.8321422G>A	rs2241592	0.14944
NM_001031.5(RPS28):c.87+75T>C	rs4147645	0.11690
NC_000019.10:g.8321483C>T	rs2241591	0.09106
NM_001031.5(RPS28):c.39+20T>G	rs73495502

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