"BloodGenetics"[submitter] AND "SLC11A2"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2446381	NM_000617.3(SLC11A2):c.675+35A>G	SLC11A2	Single nucleotide variant (intron variant)	Microcytic anemia with liver iron overload	GPathogenic
Select item 800819	NM_000617.3(SLC11A2):c.223G>A (p.Gly75Arg)	SLC11A2 (G104R +3 more)	Single nucleotide variant (missense variant +1 more)	Microcytic anemia with liver iron overload	GPathogenic