List of variants reported as pathogenic for hypochromic anemia

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000617.3(SLC11A2):c.635G>T (p.Gly212Val)	rs121918367	0.00003
NM_000617.3(SLC11A2):c.1197G>C (p.Glu399Asp)	rs121918365	0.00001
NM_000617.3(SLC11A2):c.1246C>T (p.Arg416Cys)	rs121918366
NM_000617.3(SLC11A2):c.223G>A (p.Gly75Arg)	rs1592380743
NM_000617.3(SLC11A2):c.310-5_310-3del	rs1399911403
NM_000617.3(SLC11A2):c.341_343del (p.Val114del)	rs2136280484
NM_000617.3(SLC11A2):c.675+35A>G
NM_182915.3(STEAP3):c.330C>A (p.Cys110Ter)	rs587776963

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