Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1800562
rs1800562
0.100 GeneticVariation BEFREE In conclusion, the combination of high red meat consumption, low menstrual blood loss and the HFE C282Y mutation may protect from iron deficiency in women of childbearing age. 24663082

2014

dbSNP: rs1800562
rs1800562
0.100 GeneticVariation BEFREE However, high-level expression of a liver-specific Hfe transgene carrying the mouse equivalent of the common HFE C282Y human disease-causing mutation (murine C294Y) did not cause iron deficiency. 20837779

2010

dbSNP: rs1800562
rs1800562
0.100 GeneticVariation BEFREE Iron deficiency and frequency of HFE C282Y gene mutation in Brazilian blood donors. 19747287

2009

dbSNP: rs1800562
rs1800562
0.100 GeneticVariation BEFREE Iron absorption is decreased in some patients with hemochromatosis and HFE C282Y homozygosity after bariatric surgery, but their risk of developing iron deficiency may be diminished. 15603661

2005

dbSNP: rs1800562
rs1800562
0.100 GeneticVariation BEFREE Prevalence of non-anaemic iron deficiency was significantly lower among female carriers of the C282Y mutation compared with HFE wild types. 12614226

2003

dbSNP: rs1800562
rs1800562
0.100 GeneticVariation BEFREE DMT-1 expression in C282Y homozygote subjects is consistent with the hypothesis of a "paradoxical" duodenal iron deficiency in hereditary hemochromatosis. 12547214

2003

dbSNP: rs1800562
rs1800562
0.100 GeneticVariation BEFREE C282Y and H63D +/- may protect against iron deficiency. 14642607

2003

dbSNP: rs1800562
rs1800562
0.100 GeneticVariation BEFREE Our observations suggest that the protective effect of C282Y heterozygosity against iron deficiency may be less significant than other environmental (e.g., iron-rich diet) or genetic factors. 11358395

2001

dbSNP: rs1800562
rs1800562
0.100 GeneticVariation BEFREE Homozygosity for C282Y and conditions of iron deficiency result in a downregulation of Hfe. 10772870

2000

dbSNP: rs1800562
rs1800562
0.100 GeneticVariation BEFREE In the younger age group, C282Y wild-type women did not have significantly increased serum iron, transferrin saturation, or hemoglobin values, and were not protected from developing iron deficiency, compared with women of the same age with the wild-type genotype. 10657371

2000

dbSNP: rs1800562
rs1800562
0.100 GeneticVariation BEFREE Our data provide evidence for a protective role of the C282Y mutation in the HFE gene against iron deficiency in young women and suggest that a more efficient utilization of nutritional iron may have contributed to the high prevalence of the mutation in Caucasian populations. 9836708

1998

dbSNP: rs1799945
rs1799945
0.030 GeneticVariation BEFREE Our findings suggest that selective pressure by mild iron deficiency contributes to the high frequencies of the p.H63D variant. 30827762

2019

dbSNP: rs1799945
rs1799945
0.030 GeneticVariation BEFREE Homozygocity for C in rs1799945 was associated with iron deficiency in women. 26597663

2016

dbSNP: rs1799945
rs1799945
0.030 GeneticVariation BEFREE C282Y and H63D +/- may protect against iron deficiency. 14642607

2003

dbSNP: rs1303530299
rs1303530299
0.020 GeneticVariation BEFREE In conclusion, the combination of high red meat consumption, low menstrual blood loss and the HFE C282Y mutation may protect from iron deficiency in women of childbearing age. 24663082

2014

dbSNP: rs1303530299
rs1303530299
0.020 GeneticVariation BEFREE This SNP along with the C282Y mutation explained significant differences in the distribution of individuals in three iron-related clinical phenotypes (normal, iron deficient and iron deficiency anaemic). 23324578

2013

dbSNP: rs1143627
rs1143627
0.010 GeneticVariation BEFREE ABO (rs505922) and IL1B (rs1143627) may affect H pylori infection susceptibility, and IL1B (rs1143627) may also influence ID risk in infected children. 28727656

2018

dbSNP: rs505922
rs505922
ABO
0.010 GeneticVariation BEFREE ABO (rs505922) and IL1B (rs1143627) may affect H pylori infection susceptibility, and IL1B (rs1143627) may also influence ID risk in infected children. 28727656

2018

dbSNP: rs2201841
rs2201841
0.010 GeneticVariation BEFREE The rs2201841 showed to be a risk factor for the development of iron deficiency (<i>P</i> = 0.0388, OR = 6.1837). 28210080

2017

dbSNP: rs104894347
rs104894347
0.010 GeneticVariation BEFREE We previously demonstrated that the combination of iron deficiency and a knock-in R176Q FGF23 mutation in mature mice induced FGF23 expression and hypophosphatemia that paralleled the late-onset ADHR phenotype. 23873717

2014

dbSNP: rs28940298
rs28940298
VHL
0.010 GeneticVariation BEFREE Studies including 16 additional VHL(R200W) homozygotes with low ferritin indicated that iron deficiency enhanced the induction effect of VHL(R200W) for 50 genes including hemoglobin synthesis loci but suppressed the effect for 107 genes enriched for HIF-2 targets. 23993337

2014

dbSNP: rs855791
rs855791
0.010 GeneticVariation BEFREE In 545 children below 5 years of age from rural southern Rwanda, we assessed the role of iron deficiency (ID) and of the TMPRSS6 736(V) (rs855791) allele, known to reduce iron status and haemoglobin (Hb) levels, in anaemia and Hb concentrations. 24175968

2014

dbSNP: rs11549465
rs11549465
0.010 GeneticVariation BEFREE Moreover, the HIF-1α(Pro-582-Ser) polymorphism protected regular blood donors from developing iron deficiency and anaemia and predicted uninterrupted donation activity. 24120591

2013

dbSNP: rs3811647
rs3811647
TF
0.010 GeneticVariation BEFREE Variants rs3811647 in TF and rs7385804 in TFR2 were associated with reduced SI, serum transferrin and transferrin saturation levels; however, these variants were not associated with iron deficiency or anemia risk. 22323359

2012

dbSNP: rs7385804
rs7385804
0.010 GeneticVariation BEFREE Variants rs3811647 in TF and rs7385804 in TFR2 were associated with reduced SI, serum transferrin and transferrin saturation levels; however, these variants were not associated with iron deficiency or anemia risk. 22323359

2012