ClinVar Miner

List of variants reported as uncertain significance for hypochromic anemia

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 63
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001063.4(TF):c.829G>A (p.Gly277Ser) rs1799899 0.04529
NM_000617.3(SLC11A2):c.*1058G>A rs41398049 0.00427
NM_000617.3(SLC11A2):c.504A>G (p.Ser168=) rs145155499 0.00145
NM_000617.3(SLC11A2):c.197G>A (p.Ser66Asn) rs141728916 0.00118
NM_000617.3(SLC11A2):c.*11G>A rs201382454 0.00091
NM_000617.3(SLC11A2):c.15T>C (p.Pro5=) rs192462172 0.00040
NM_000617.3(SLC11A2):c.*1949A>G rs72561485 0.00036
NM_000617.3(SLC11A2):c.1425C>T (p.Gly475=) rs139057918 0.00032
NM_000617.3(SLC11A2):c.1258A>G (p.Ile420Val) rs148582995 0.00031
NM_000617.3(SLC11A2):c.*716G>A rs571129669 0.00029
NM_000617.3(SLC11A2):c.*1795G>A rs750648046 0.00022
NM_000617.3(SLC11A2):c.*1057C>T rs767436028 0.00021
NM_000617.3(SLC11A2):c.*2332A>T rs575495762 0.00014
NM_000617.3(SLC11A2):c.1032C>G (p.Leu344=) rs370750890 0.00013
NM_000617.3(SLC11A2):c.-50G>A rs886049570 0.00010
NM_000617.3(SLC11A2):c.-39G>A rs751410203 0.00009
NM_000617.3(SLC11A2):c.*1739C>T rs766628921 0.00008
NM_000617.3(SLC11A2):c.*1599C>T rs886049559 0.00006
NM_000617.3(SLC11A2):c.*415G>A rs765348165 0.00006
NM_000617.3(SLC11A2):c.1584A>G (p.Gln528=) rs761505350 0.00006
NM_000617.3(SLC11A2):c.290G>C (p.Gly97Ala) rs138686455 0.00005
NM_000617.3(SLC11A2):c.932A>G (p.Asn311Ser) rs769742722 0.00005
NM_001174125.2(SLC11A2):c.49+1746C>T rs886763852 0.00005
NM_000617.3(SLC11A2):c.1663G>A (p.Ala555Thr) rs550969378 0.00004
NM_000617.3(SLC11A2):c.523C>T (p.Leu175=) rs373590039 0.00004
NM_000617.3(SLC11A2):c.*1007A>G rs886049560 0.00003
NM_000617.3(SLC11A2):c.*1559G>T rs777649881 0.00003
NM_000617.3(SLC11A2):c.*1902C>G rs886049558 0.00003
NM_000617.3(SLC11A2):c.1206G>A (p.Leu402=) rs761054843 0.00003
NM_000617.3(SLC11A2):c.514A>G (p.Ile172Val) rs886049568 0.00003
NM_000617.3(SLC11A2):c.*1360A>G rs573581505 0.00002
NM_000617.3(SLC11A2):c.*420G>A rs886049564 0.00002
NM_000617.3(SLC11A2):c.1049C>T (p.Ser350Leu) rs376365060 0.00002
NM_000617.3(SLC11A2):c.921C>T (p.Ser307=) rs762100462 0.00002
NM_000617.3(SLC11A2):c.*1367T>C rs1235162595 0.00001
NM_000617.3(SLC11A2):c.*1615T>C rs557225035 0.00001
NM_000617.3(SLC11A2):c.*32A>G rs886049565 0.00001
NM_000617.3(SLC11A2):c.*985G>A rs886049562 0.00001
NM_000617.3(SLC11A2):c.*986C>A rs886049561 0.00001
NM_000617.3(SLC11A2):c.-96C>T rs747408183 0.00001
NM_000617.3(SLC11A2):c.1197G>C (p.Glu399Asp) rs121918365 0.00001
NM_000617.3(SLC11A2):c.1511A>G (p.His504Arg) rs1229345464 0.00001
NM_000617.3(SLC11A2):c.1596A>C (p.Ala532=) rs760783598 0.00001
NM_000617.3(SLC11A2):c.1655C>T (p.Thr552Ile) rs1469622244 0.00001
NM_000617.3(SLC11A2):c.647C>T (p.Thr216Ile) rs886049567 0.00001
NM_001174125.2(SLC11A2):c.49+1791C>T rs920922103 0.00001
NM_000617.3(SLC11A2):c.*1444C>T rs946003076
NM_000617.3(SLC11A2):c.*1466dup rs561463670
NM_000617.3(SLC11A2):c.*1752dup rs755515112
NM_000617.3(SLC11A2):c.*2083_*2084del rs886049557
NM_000617.3(SLC11A2):c.*2289G>T rs867212578
NM_000617.3(SLC11A2):c.*2320del rs141968385
NM_000617.3(SLC11A2):c.*295G>A rs1940770079
NM_000617.3(SLC11A2):c.*970A>G rs886049563
NM_000617.3(SLC11A2):c.-38-3C>T rs886049569
NM_000617.3(SLC11A2):c.-39+12G>A rs1944384418
NM_000617.3(SLC11A2):c.1421+8T>A rs886049566
NM_000617.3(SLC11A2):c.1576-7C>G rs1940818391
NM_000617.3(SLC11A2):c.436C>G (p.Arg146Gly) rs774857007
NM_000617.3(SLC11A2):c.578C>T (p.Thr193Ile)
NM_000617.3(SLC11A2):c.715G>A (p.Gly239Ser) rs1592344306
NM_000617.3(SLC11A2):c.828C>G (p.Val276=) rs754854640
NM_001174125.2(SLC11A2):c.49+1757C>T rs1057516023

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.