List of variants reported as uncertain significance for anemia by Clinical Genomics Laboratory, Washington University in St. Louis

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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_001081.4(CUBN):c.3356T>C (p.Leu1119Ser)	rs141164907	0.00089
NM_000186.4(CFH):c.3152C>T (p.Pro1051Leu)
NM_001081.4(CUBN):c.6905C>T (p.Pro2302Leu)

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