List of variants in gene RPS17 reported as likely benign for anemia

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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_001021.6(RPS17):c.159T>C (p.Tyr53=)	rs6991	0.25775
NM_001021.6(RPS17):c.312A>G (p.Glu104=)	rs1049218128	0.02409
NM_001021.6(RPS17):c.328-7G>A	rs975130647	0.00215
NM_001021.6(RPS17):c.126C>T (p.Pro42=)
NM_001021.6(RPS17):c.390G>A (p.Thr130=)
NM_001021.6(RPS17):c.39C>T (p.Ala13=)
NM_001021.6(RPS17):c.45C>T (p.Val15=)

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