List of variants in gene combination MIR6797, RPS19 reported as likely 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001022.4(RPS19):c.357-17C>T	rs782356785	0.00005
NM_001022.4(RPS19):c.357-6C>T	rs529093944	0.00001
NM_001022.4(RPS19):c.357-10C>T

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