List of variants reported as likely benign for anemia by St. Jude Molecular Pathology, St. Jude Children's Research Hospital

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_005236.3(ERCC4):c.2117T>C (p.Ile706Thr)	rs1800069	0.00190
NM_000136.3(FANCC):c.178G>A (p.Val60Ile)	rs138629441	0.00091

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