List of variants in gene RPS7 reported as likely pathogenic for hematologic disorder

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001011.4(RPS7):c.-19+1G>A	rs1064796859
NM_001011.4(RPS7):c.-19+1G>C	rs1064796859
NM_001011.4(RPS7):c.508-3T>G	rs1572360944
NM_001011.4(RPS7):c.65_68del (p.Gly22fs)
NM_001011.4(RPS7):c.75+1G>T

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