List of variants in gene SLC11A2 reported as benign for anemia, hypochromic microcytic with iron overload

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 24

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HGVS	dbSNP	gnomAD frequency
NM_000617.3(SLC11A2):c.*1031G>A	rs150909	0.90829
NM_000617.3(SLC11A2):c.1576-14A>G	rs161044	0.90828
NM_000617.3(SLC11A2):c.-110G>T	rs6580779	0.90822
NM_000617.3(SLC11A2):c.35-498A>C	rs445520	0.90819
NM_000617.3(SLC11A2):c.*1876T>C	rs149411	0.53019
NM_000617.3(SLC11A2):c.34+11G>A	rs427020	0.46181
NM_000617.3(SLC11A2):c.*390G>A	rs224446	0.16154
NM_000617.3(SLC11A2):c.*358A>G	rs2285230	0.14298
NM_000617.3(SLC11A2):c.1254T>C (p.Ile418=)	rs1048230	0.14293
NM_000617.3(SLC11A2):c.*1273G>A	rs11169654	0.14282
NM_000617.3(SLC11A2):c.607+12G>A	rs224454	0.14139
NM_000617.3(SLC11A2):c.*1215A>C	rs17125172	0.05066
NM_000617.3(SLC11A2):c.34+6T>G	rs17216107	0.01065
NM_000617.3(SLC11A2):c.*1261G>A	rs60725885	0.00753
NM_000617.3(SLC11A2):c.*872A>C	rs73297974	0.00752
NM_000617.3(SLC11A2):c.-78G>A	rs2301528	0.00652
NM_000617.3(SLC11A2):c.*1486G>T	rs116731209	0.00538
NM_000617.3(SLC11A2):c.*789G>A	rs79206015	0.00538
NM_000617.3(SLC11A2):c.184T>C (p.Tyr62His)	rs17222470	0.00534
NM_000617.3(SLC11A2):c.625G>A (p.Ala209Thr)	rs115874705	0.00453
NM_000617.3(SLC11A2):c.893T>C (p.Ile298Thr)	rs17216051	0.00155
NM_000617.3(SLC11A2):c.-39+5G>C	rs180796770	0.00105
NM_000617.3(SLC11A2):c.255G>T (p.Leu85=)	rs17216072	0.00041
NM_000617.3(SLC11A2):c.309+44A>C	rs224589

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