ClinVar Miner

List of variants studied for Hypochromic microcytic anemia with iron overload by Illumina Clinical Services Laboratory,Illumina

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Total variants: 56
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HGVS dbSNP
NM_000617.3(SLC11A2):c.-110G>T rs6580779
NM_000617.3(SLC11A2):c.-38-3C>T rs886049569
NM_000617.3(SLC11A2):c.-39G>A rs751410203
NM_000617.3(SLC11A2):c.-50G>A rs886049570
NM_000617.3(SLC11A2):c.-78G>A rs2301528
NM_000617.3(SLC11A2):c.1197G>C (p.Glu399Asp) rs121918365
NM_000617.3(SLC11A2):c.1206G>A (p.Leu402=) rs761054843
NM_000617.3(SLC11A2):c.1254T>C (p.Ile418=) rs1048230
NM_000617.3(SLC11A2):c.1258A>G (p.Ile420Val) rs148582995
NM_000617.3(SLC11A2):c.1348-10T>C rs189993499
NM_000617.3(SLC11A2):c.1421+8T>A rs886049566
NM_000617.3(SLC11A2):c.1425C>T (p.Gly475=) rs139057918
NM_000617.3(SLC11A2):c.1576-14A>G rs161044
NM_000617.3(SLC11A2):c.1584A>G (p.Gln528=) rs761505350
NM_000617.3(SLC11A2):c.1596A>C (p.Ala532=) rs760783598
NM_000617.3(SLC11A2):c.1663G>A (p.Ala555Thr) rs550969378
NM_000617.3(SLC11A2):c.197G>A (p.Ser66Asn) rs141728916
NM_000617.3(SLC11A2):c.34+11G>A rs427020
NM_000617.3(SLC11A2):c.436C>G (p.Arg146Gly) rs774857007
NM_000617.3(SLC11A2):c.504A>G (p.Ser168=) rs145155499
NM_000617.3(SLC11A2):c.514A>G (p.Ile172Val) rs886049568
NM_000617.3(SLC11A2):c.607+12G>A rs224454
NM_000617.3(SLC11A2):c.625G>A (p.Ala209Thr) rs115874705
NM_000617.3(SLC11A2):c.647C>T (p.Thr216Ile) rs886049567
NM_000617.3(SLC11A2):c.921C>T (p.Ser307=) rs762100462
NM_000617.3(SLC11A2):c.932A>G (p.Asn311Ser) rs769742722
NM_001174125.2(SLC11A2):c.49+1746C>T rs886763852
NM_001174125.2(SLC11A2):c.49+1757C>T rs1057516023
NM_001174126.1(SLC11A2):c.1629+1027A>G rs886049563
NM_001174126.1(SLC11A2):c.1629+1042G>A rs886049562
NM_001174126.1(SLC11A2):c.1629+1043C>A rs886049561
NM_001174126.1(SLC11A2):c.1629+1064A>G rs886049560
NM_001174126.1(SLC11A2):c.1629+1088G>A rs150909
NM_001174126.1(SLC11A2):c.1629+1272A>C rs17125172
NM_001174126.1(SLC11A2):c.1629+1318G>A rs60725885
NM_001174126.1(SLC11A2):c.1629+1330G>A rs11169654
NM_001174126.1(SLC11A2):c.1629+1522dup rs561463670
NM_001174126.1(SLC11A2):c.1629+1543G>T rs116731209
NM_001174126.1(SLC11A2):c.1629+1616G>T rs777649881
NM_001174126.1(SLC11A2):c.1629+1656C>T rs886049559
NM_001174126.1(SLC11A2):c.1629+1800dup rs755515112
NM_001174126.1(SLC11A2):c.1629+1933T>C rs149411
NM_001174126.1(SLC11A2):c.1629+1959C>G rs886049558
NM_001174126.1(SLC11A2):c.1629+2006A>G rs72561485
NM_001174126.1(SLC11A2):c.1629+210A>G rs146016854
NM_001174126.1(SLC11A2):c.1629+2140_1629+2141del rs886049557
NM_001174126.1(SLC11A2):c.1629+2346G>T rs867212578
NM_001174126.1(SLC11A2):c.1629+2377del rs141968385
NM_001174126.1(SLC11A2):c.1629+415A>G rs2285230
NM_001174126.1(SLC11A2):c.1629+447G>A rs224446
NM_001174126.1(SLC11A2):c.1629+472G>A rs765348165
NM_001174126.1(SLC11A2):c.1629+477G>A rs886049564
NM_001174126.1(SLC11A2):c.1629+603G>A rs193030246
NM_001174126.1(SLC11A2):c.1629+68G>A rs201382454
NM_001174126.1(SLC11A2):c.1629+89A>G rs886049565
NM_001174126.1(SLC11A2):c.1629+929A>C rs73297974

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