ClinVar Miner

List of variants in gene RPS17 reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001021.6(RPS17):c.312A>G (p.Glu104=)	rs1049218128	0.02409
NM_001021.6(RPS17):c.328-7G>A	rs975130647	0.00215

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