Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893662
rs104893662
SLC40A1
0.800 GeneticVariation UNIPROT Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis. 12091366

2002
dbSNP: rs104893662
rs104893662
SLC40A1
0.800 GeneticVariation UNIPROT Recent advances in understanding haemochromatosis: a transition state. 15466004

2004
dbSNP: rs104893662
rs104893662
SLC40A1
0.800 GeneticVariation UNIPROT Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene. 11518736

2001
dbSNP: rs104893662
rs104893662
SLC40A1
0.800 GeneticVariation UNIPROT Molecular analyses of patients with hyperferritinemia and normal serum iron values reveal both L ferritin IRE and 3 new ferroportin (slc11A3) mutations. 12730114

2003
dbSNP: rs104893662
rs104893662
SLC40A1
0.800 GeneticVariation UNIPROT Genetic and clinical heterogeneity of ferroportin disease. 16351644

2005
dbSNP: rs104893662
rs104893662
SLC40A1
0.800 GeneticVariation UNIPROT Analysis of genes implicated in iron regulation in individuals presenting with primary iron overload. 15338274

2004
dbSNP: rs104893662
rs104893662
SLC40A1
0.800 GeneticVariation UNIPROT Genetic hyperferritinaemia and reticuloendothelial iron overload associated with a three base pair deletion in the coding region of the ferroportin gene (SLC11A3). 12406098

2002
dbSNP: rs104893662
rs104893662
SLC40A1
0.800 GeneticVariation UNIPROT A novel mammalian iron-regulated protein involved in intracellular iron metabolism. 10747949

2000
dbSNP: rs104893662
rs104893662
SLC40A1
0.800 GeneticVariation UNIPROT A valine deletion of ferroportin 1: a common mutation in hemochromastosis type 4. 12123233

2002
dbSNP: rs104893662
rs104893662
SLC40A1
0.800 GeneticVariation UNIPROT Autosomal dominant reticuloendothelial iron overload (HFE type 4) due to a new missense mutation in the FERROPORTIN 1 gene (SLC11A3) in a large French-Canadian family. 12857562

2003
dbSNP: rs104893662
rs104893662
SLC40A1
0.800 GeneticVariation UNIPROT A novel mutation in ferroportin1 is associated with haemochromatosis in a Solomon Islands patient. 12865285

2003
dbSNP: rs104893662
rs104893662
SLC40A1
0.800 GeneticVariation UNIPROT A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis. 11431687

2001
dbSNP: rs104893662
rs104893662
SLC40A1
0.800 GeneticVariation UNIPROT Autosomal dominant reticuloendothelial iron overload associated with a 3-base pair deletion in the ferroportin 1 gene (SLC11A3). 12091367

2002
dbSNP: rs104893663
rs104893663
SLC40A1
0.800 GeneticVariation UNIPROT A valine deletion of ferroportin 1: a common mutation in hemochromastosis type 4. 12123233

2002
dbSNP: rs104893663
rs104893663
SLC40A1
0.800 GeneticVariation UNIPROT Autosomal dominant reticuloendothelial iron overload (HFE type 4) due to a new missense mutation in the FERROPORTIN 1 gene (SLC11A3) in a large French-Canadian family. 12857562

2003
dbSNP: rs104893663
rs104893663
SLC40A1
0.800 GeneticVariation UNIPROT Recent advances in understanding haemochromatosis: a transition state. 15466004

2004
dbSNP: rs104893663
rs104893663
SLC40A1
0.800 GeneticVariation UNIPROT Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis. 12091366

2002
dbSNP: rs104893663
rs104893663
SLC40A1
0.800 GeneticVariation UNIPROT A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis. 11431687

2001
dbSNP: rs104893663
rs104893663
SLC40A1
0.800 GeneticVariation UNIPROT Analysis of genes implicated in iron regulation in individuals presenting with primary iron overload. 15338274

2004
dbSNP: rs104893663
rs104893663
SLC40A1
0.800 GeneticVariation UNIPROT Genetic hyperferritinaemia and reticuloendothelial iron overload associated with a three base pair deletion in the coding region of the ferroportin gene (SLC11A3). 12406098

2002
dbSNP: rs104893663
rs104893663
SLC40A1
0.800 GeneticVariation UNIPROT Genetic and clinical heterogeneity of ferroportin disease. 16351644

2005
dbSNP: rs104893663
rs104893663
SLC40A1
0.800 GeneticVariation UNIPROT Molecular analyses of patients with hyperferritinemia and normal serum iron values reveal both L ferritin IRE and 3 new ferroportin (slc11A3) mutations. 12730114

2003
dbSNP: rs104893663
rs104893663
SLC40A1
0.800 GeneticVariation UNIPROT Autosomal dominant reticuloendothelial iron overload associated with a 3-base pair deletion in the ferroportin 1 gene (SLC11A3). 12091367

2002
dbSNP: rs104893663
rs104893663
SLC40A1
0.800 GeneticVariation UNIPROT A novel mammalian iron-regulated protein involved in intracellular iron metabolism. 10747949

2000
dbSNP: rs104893663
rs104893663
SLC40A1
0.800 GeneticVariation UNIPROT Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene. 11518736

2001