ClinVar Miner

List of variants in gene SLC11A2 reported as benign for Anemia, hypochromic microcytic, with iron overload 1

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Total variants: 22
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HGVS dbSNP
NM_000617.3(SLC11A2):c.-110G>T rs6580779
NM_000617.3(SLC11A2):c.-39+5G>C
NM_000617.3(SLC11A2):c.-78G>A rs2301528
NM_000617.3(SLC11A2):c.1254T>C (p.Ile418=) rs1048230
NM_000617.3(SLC11A2):c.1576-14A>G rs161044
NM_000617.3(SLC11A2):c.184T>C (p.Tyr62His)
NM_000617.3(SLC11A2):c.255G>T (p.Leu85=)
NM_000617.3(SLC11A2):c.34+11G>A rs427020
NM_000617.3(SLC11A2):c.34+6T>G
NM_000617.3(SLC11A2):c.607+12G>A rs224454
NM_000617.3(SLC11A2):c.625G>A (p.Ala209Thr) rs115874705
NM_000617.3(SLC11A2):c.893T>C (p.Ile298Thr)
NM_001174126.2(SLC11A2):c.1629+1088G>A rs150909
NM_001174126.2(SLC11A2):c.1629+1272A>C rs17125172
NM_001174126.2(SLC11A2):c.1629+1318G>A rs60725885
NM_001174126.2(SLC11A2):c.1629+1330G>A rs11169654
NM_001174126.2(SLC11A2):c.1629+1543G>T rs116731209
NM_001174126.2(SLC11A2):c.1629+1933T>C rs149411
NM_001174126.2(SLC11A2):c.1629+415A>G rs2285230
NM_001174126.2(SLC11A2):c.1629+447G>A rs224446
NM_001174126.2(SLC11A2):c.1629+846G>A
NM_001174126.2(SLC11A2):c.1629+929A>C rs73297974

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