List of variants in gene SRP72 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_006947.4(SRP72):c.1640+6dup	rs572508224	0.00334
NM_006947.4(SRP72):c.1704A>G (p.Pro568=)	rs41280351	0.00053
NM_006947.4(SRP72):c.1698T>C (p.Tyr566=)	rs145347209	0.00037
NM_006947.4(SRP72):c.1225-6G>A	rs752594366	0.00002

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