List of variants in gene RPS17 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001021.6(RPS17):c.327+80G>A	rs990557809	0.01433
NC_000015.10:g.82540460G>A	rs575115395	0.00080
NM_001021.6(RPS17):c.3+132C>G	rs542153649

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