|
rs1800562
|
|
|
0.800 |
GeneticVariation |
BEFREE |
The exon 5 variant was identified in one of 13 patients referred for a molecular diagnosis of hereditary haemochromatosis (HH), who tested negative for the known C282Y and H63D mutations.
|
10401000 |
1999 |
|
rs1800562
|
|
|
0.800 |
GeneticVariation |
BEFREE |
Homozygosity for the C282Y mutation of the HFE gene is a highly significant risk factor for the development of hereditary hemochromatosis (HH) and the majority of patients with HH have this genotype.
|
11531973 |
2001 |
|
rs1800562
|
|
|
0.800 |
GeneticVariation |
BEFREE |
We observed a high frequency of the H63D mutation in both the control group and patients, whereas the main genotypes implicated in HH in our series were H63D homozygous and H63D/C282Y compound heterozygous.
|
15727249 |
2004 |
|
rs1800562
|
|
|
0.800 |
GeneticVariation |
BEFREE |
The recent identification of 2 mutations in the HFE gene related to hereditary haemochromatosis (Cys282Tyr and His63Asp) provided an opportunity to test whether they are associated with hepatic iron accumulation and the activity and severity of liver disease in hepatitis C virus (HCV) infection.
|
10692680 |
2000 |
|
rs1800562
|
|
|
0.800 |
GeneticVariation |
BEFREE |
Epidemiological studies have revealed a strict association between hereditary haemochromatosis and C282Y homozygosis or C282Y/H63D compound heterozygosis, suggesting that these mutations may provide a useful tool for diagnosis.
|
15061375 |
2004 |
|
rs1800562
|
|
|
0.800 |
GeneticVariation |
BEFREE |
Hence, homozygosity for p.C282Y is not sufficient to diagnose HH.
|
26153218 |
2016 |
|
rs1800562
|
|
|
0.800 |
GeneticVariation |
BEFREE |
Statistically significant differences were observed for genotype distribution of C282Y (P < 0.001) and H63D (P = 0.013) between the general population and the patients diagnosed with HH.
|
27173269 |
2016 |
|
rs1800562
|
|
|
0.800 |
GeneticVariation |
BEFREE |
A systematic review of patients with HH over a 2-year period within a defined UK region has revealed that only 1.2% of adult C282Y homozygotes have been diagnosed with iron overload and received treatment.
|
12436244 |
2002 |
|
rs1800562
|
|
|
0.800 |
GeneticVariation |
BEFREE |
C282Y and H63D are the main mutations related to hereditary hemochromatosis; these mutations have been reported to be associated with increased risk of developing diabetes mellitus type 2 (DM2).
|
19876870 |
2009 |
|
rs1800562
|
|
|
0.800 |
GeneticVariation |
BEFREE |
Most persons who are homozygous for C282Y, the HFE allele most commonly asssociated with hereditary hemochromatosis, have elevated levels of serum ferritin and transferrin saturation.
|
18199861 |
2008 |
|
rs1800562
|
|
|
0.800 |
GeneticVariation |
BEFREE |
The most common cause of hereditary hemochromatosis is a C282Y mutation in the HFE gene.
|
31582009 |
2019 |
|
rs1800562
|
|
|
0.800 |
GeneticVariation |
BEFREE |
The most common form of HH is caused by mutations in the HFE gene, with most cases of HH presenting in patients who are homozygous for the Cys282Tyr mutation.
|
20010968 |
2010 |
|
rs1800562
|
|
|
0.800 |
GeneticVariation |
BEFREE |
Since in the general Turkish population, the C282Y mutation is not found and the H63D mutation is of high frequency, we aimed to determine mutations in the HFE genes in our patients with HH.
|
15871018 |
2005 |
|
rs1800562
|
|
|
0.800 |
GeneticVariation |
BEFREE |
DMT1, IREG1, and HFE mRNA were measured in duodenal tissue of C282Y homozygous HH patients, in ID patients negative for the C282Y mutation with a serum ferritin concentration less than 20 microg/l, and in controls negative for C282Y and H63D mutations with normal iron indices, using real time polymerase chain reaction.
|
15247188 |
2004 |
|
rs1800562
|
|
|
0.800 |
GeneticVariation |
BEFREE |
Therefore, further efforts to characterize the unscreened part of the HFE gene or other loci should be taken to identify the potential genetic factors causing HH in the C282Y-negative patients.
|
10953957 |
2000 |
|
rs1800562
|
|
|
0.800 |
GeneticVariation |
BEFREE |
To determine the contribution of the C282Y and H63D mutations in the HFE gene to clinical expression of hereditary hemochromatosis.
|
11399207 |
2008 |
|
rs1800562
|
|
|
0.800 |
GeneticVariation |
BEFREE |
Homozygosity for the C282Y mutation in the HFE gene is strongly associated with hereditary hemochromatosis.
|
12210292 |
2002 |
|
rs1800562
|
|
|
0.800 |
GeneticVariation |
BEFREE |
The high C282Y allele frequency in the Irish population together with its close linkage to HH indicate that C282Y genotyping is the preferred screening strategy for this disease in Ireland.
|
11551098 |
2001 |
|
rs1800562
|
|
|
0.800 |
GeneticVariation |
BEFREE |
The detection rate for homozygous C282Y HH for male patients with both SF ≥ 300 μg/L and Tsat >50% was 18.8% (52/272) and 16.3% (68/415) for female patients with both SF ≥ 200 μg/L and Tsat >40%.
|
25540266 |
2015 |
|
rs1800562
|
|
|
0.800 |
GeneticVariation |
BEFREE |
Together, these data shed light on the molecular mechanisms involved in HFE C282Y-related HH and open new perspectives on the use of orally active chemical chaperones as a therapeutic approach for HH.
|
17626021 |
2007 |
|
rs1800562
|
|
|
0.800 |
GeneticVariation |
BEFREE |
Type 1 hereditary hemochromatosis is a common disorder of iron overload occurring in individuals homozygous for the C282Y HFE gene mutation.
|
16315134 |
2005 |
|
rs1800562
|
|
|
0.800 |
GeneticVariation |
BEFREE |
The patient was found to carry the HFE C282Y and H63D mutations, which are associated with hereditary hemochromatosis, and the alpha(1)-antitrypsin PiZ variant.
|
15514099 |
2005 |
|
rs1800562
|
|
|
0.800 |
GeneticVariation |
BEFREE |
In the UK, 90% of patients with hereditary haemochromatosis (HH) are homozygous for HFE C282Y, as are one in 150 people in the general population.
|
12846904 |
2003 |
|
rs1800562
|
|
|
0.800 |
GeneticVariation |
BEFREE |
Our findings indicate that underdiagnosis of HH may be due to the non-specific nature of early symptoms and less frequently to the incomplete penetrance of the C282Y mutation.
|
12077102 |
2002 |
|
rs1800562
|
|
|
0.800 |
GeneticVariation |
BEFREE |
An expected significant association between HH and HLA-A3 was observed, which was found to be in linkage disequilibrium with the C282Y mutation.
|
9510559 |
1998 |