List of variants in gene RPS7 reported as benign for anemia

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001011.4(RPS7):c.508-12C>A	rs2071639	0.12923
NM_001011.4(RPS7):c.-47G>T	rs11558965	0.05197
NM_001011.4(RPS7):c.-36A>C	rs17552296	0.00303
NM_001011.4(RPS7):c.*31C>T	rs191506876	0.00014
NM_001011.4(RPS7):c.459C>G (p.Leu153=)	rs777622518	0.00011
NM_001011.4(RPS7):c.276C>G (p.Val92=)	rs61730448	0.00008
NM_001011.4(RPS7):c.435C>T (p.Arg145=)	rs142207795	0.00004
NM_001011.4(RPS7):c.99C>T (p.Asn33=)	rs61732234	0.00002
NM_001011.4(RPS7):c.-19+13C>T	rs530845583
NM_001011.4(RPS7):c.148-7del
NM_001011.4(RPS7):c.357-16dup
NM_001011.4(RPS7):c.357-3dup	rs140914434
NM_001011.4(RPS7):c.508-16C>A

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