ClinVar Miner

List of variants reported as uncertain significance for Hemochromatosis type 1

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Total variants: 52
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HGVS dbSNP gnomAD frequency
NM_000410.4(HFE):c.187C>G (p.His63Asp) rs1799945 0.10170
NM_000410.4(HFE):c.*871C>T rs62625357 0.03584
NM_000410.4(HFE):c.*801T>C rs62625356 0.03341
NM_000410.4(HFE):c.193A>T (p.Ser65Cys) rs1800730 0.00992
NM_000410.4(HFE):c.*988G>A rs143278243 0.00983
NM_000410.4(HFE):c.*991C>T rs148307737 0.00982
NM_000410.4(HFE):c.*61C>T rs62625349 0.00793
NM_000410.4(HFE):c.*403T>C rs62625351 0.00761
NM_000410.4(HFE):c.1026C>T (p.Tyr342=) rs35201683 0.00515
NM_000410.4(HFE):c.*296A>T rs62625350 0.00356
NM_000410.4(HFE):c.*281C>T rs140664305 0.00151
NM_000410.4(HFE):c.*578T>C rs539558655 0.00139
NM_000410.4(HFE):c.502G>C (p.Glu168Gln) rs146519482 0.00102
NM_000410.4(HFE):c.*459C>T rs569199586 0.00100
NM_000410.4(HFE):c.*155C>T rs192228238 0.00078
NM_000410.4(HFE):c.*746G>T rs62625355 0.00078
NM_000410.4(HFE):c.18G>C (p.Arg6Ser) rs149342416 0.00072
NM_000410.4(HFE):c.1006+14A>G rs201262562 0.00068
NM_000410.4(HFE):c.*603C>T rs62625353 0.00063
NM_000410.4(HFE):c.884T>C (p.Val295Ala) rs143175221 0.00056
NM_000410.4(HFE):c.*198C>T rs544604880 0.00048
NM_000410.4(HFE):c.21G>A (p.Pro7=) rs114758821 0.00045
NM_000410.4(HFE):c.50C>T (p.Thr17Ile) rs143662783 0.00044
NM_000410.4(HFE):c.68G>A (p.Arg23His) rs148161858 0.00032
NM_000410.4(HFE):c.*744G>C rs775050499 0.00031
NM_000410.4(HFE):c.*417C>T rs118079331 0.00027
NM_000410.4(HFE):c.496A>G (p.Lys166Glu) rs144170531 0.00023
NM_000410.4(HFE):c.157G>A (p.Val53Met) rs28934889 0.00022
NM_000410.4(HFE):c.*918A>G rs192191139 0.00014
NM_000410.4(HFE):c.670C>T (p.Arg224Trp) rs144797937 0.00013
NM_000410.4(HFE):c.*957T>C rs886061284 0.00008
NM_003227.4(TFR2):c.1118G>A (p.Gly373Asp) rs202221581 0.00006
NM_014585.6(SLC40A1):c.695C>A (p.Ala232Asp) rs760236238 0.00006
NM_000410.4(HFE):c.*199G>A rs766844750 0.00005
NM_000410.4(HFE):c.*120C>T rs573474865 0.00004
NM_000410.4(HFE):c.175G>A (p.Val59Met) rs111033557 0.00004
NM_000410.4(HFE):c.40C>G (p.Leu14Val) rs201657128 0.00004
NM_000410.4(HFE):c.676C>T (p.Arg226Trp) rs781516027 0.00004
NM_000410.3(HFE):c.-96G>C rs768639966 0.00003
NM_000410.4(HFE):c.-7T>C rs369807746 0.00003
NM_000410.4(HFE):c.212G>A (p.Arg71Gln) rs776741897 0.00002
NM_000410.4(HFE):c.*301C>A rs373610457 0.00001
NM_000410.4(HFE):c.*517A>G rs886061283 0.00001
NM_000410.4(HFE):c.*625C>T rs538372302 0.00001
NM_000410.4(HFE):c.196C>T (p.Arg66Cys) rs747739169 0.00001
NM_000410.4(HFE):c.766G>A (p.Val256Ile) rs202068193 0.00001
NM_000410.4(HFE):c.*426T>C rs1762937555
NM_000410.4(HFE):c.*838T>C rs1762963332
NM_000410.4(HFE):c.200G>T (p.Arg67Leu) rs139523708
NM_000410.4(HFE):c.202G>A (p.Val68Met) rs776668429
NM_000410.4(HFE):c.707C>T (p.Thr236Ile) rs557062229
NM_000410.4(HFE):c.976T>A (p.Phe326Ile) rs1214213770

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