ClinVar Miner

List of variants reported as benign for hypochromic anemia

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
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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