List of variants reported as uncertain significance for anemia by Institute for Medical Genetics and Human Genetics, Charité - Universitätsmedizin Berlin

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000617.3(SLC11A2):c.578C>T (p.Thr193Ile)
NM_001018115.3(FANCD2):c.2606-9A>G
NM_001018115.3(FANCD2):c.3713T>A (p.Met1238Lys)

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