|
rs1554317002
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
|
rs1555307370
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs1555738475
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs1564494285
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs1566304640
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
|
rs587784347
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
|
rs781214034
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
|
rs1800562
|
|
|
0.030 |
GeneticVariation |
BEFREE |
We investigated the role of HFE C282Y, H63D, and TMPRSS6 A736V variants in the pathogenesis of iron deficiency anemia (IDA) in celiac disease (CD) patients, at diagnosis and after 1 year of gluten-free diet (GFD).
|
29194702 |
2018 |
|
rs855791
|
|
|
0.030 |
GeneticVariation |
BEFREE |
At follow-up, A736V was significantly increased in IDA persistent than in IDA not persistent (57.7% vs 35.2%, P < .0001).
|
29194702 |
2018 |
|
rs855791
|
|
|
0.030 |
GeneticVariation |
BEFREE |
Our study suggests homozygosity for TMPRSS6 rs855791 C genotype has a protective role against IDA in women at reproductive age, especially in those with menorrhagia.
|
24782651 |
2014 |
|
rs855791
|
|
|
0.030 |
GeneticVariation |
BEFREE |
To evaluate the association of genetic variants in genes involved in iron delivery and hepcidin regulation pathways with the risk of iron-deficiency anemia (IDA), the following single nucleotide polymorphisms were genotyped in 2139 unrelated elderly Chinese women: rs3811647 (TF), rs7385804 (TFR2), rs235756 (BMP2), and rs855791(V736A) and rs4820268 (TMPRSS6, encoding matriptase-2).
|
22323359 |
2012 |
|
rs1800562
|
|
|
0.030 |
GeneticVariation |
BEFREE |
The protective effect of the heterozygous genotype for HFE C282Y mutation against ID and IDA in female blood donors was also determined.
|
19747287 |
2009 |
|
rs1800562
|
|
|
0.030 |
GeneticVariation |
BEFREE |
We determined whether the rise in post-prandial serum iron is increased in fully treated patients with hereditary haemochromatosis (HFE C282Y+/+; HH) compared to iron deficiency anaemia (IDA), iron-replete heterozygous subjects (HFE C282Y+/-) and iron-replete controls (HFE C282Y-/-).
|
18276042 |
2008 |
|
rs1161457931
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We investigated the role of HFE C282Y, H63D, and TMPRSS6 A736V variants in the pathogenesis of iron deficiency anemia (IDA) in celiac disease (CD) patients, at diagnosis and after 1 year of gluten-free diet (GFD).
|
29194702 |
2018 |
|
rs1208663703
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We investigated the role of HFE C282Y, H63D, and TMPRSS6 A736V variants in the pathogenesis of iron deficiency anemia (IDA) in celiac disease (CD) patients, at diagnosis and after 1 year of gluten-free diet (GFD).
|
29194702 |
2018 |
|
rs1799945
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We investigated the role of HFE C282Y, H63D, and TMPRSS6 A736V variants in the pathogenesis of iron deficiency anemia (IDA) in celiac disease (CD) patients, at diagnosis and after 1 year of gluten-free diet (GFD).
|
29194702 |
2018 |
|
rs733655
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The aim of the study was to investigate the association of rs855791, rs4820268, rs5756506, rs2235324, rs2413450, rs2111833, rs228919, and rs733655 SNPs in TMPRSS6 gene with IDA susceptibility and iron-related clinical parameters.
|
29928945 |
2018 |
|
rs113488022
|
|
|
0.010 |
GeneticVariation |
BEFREE |
BRAF V600E mutation might be associated with right-sided tumors and subsequently related unexplained iron-deficiency anaemia (IDA) at presentation.
|
25862899 |
2015 |
|
rs121913377
|
|
|
0.010 |
GeneticVariation |
BEFREE |
BRAF V600E mutation might be associated with right-sided tumors and subsequently related unexplained iron-deficiency anaemia (IDA) at presentation.
|
25862899 |
2015 |
|
rs235756
|
|
|
0.010 |
GeneticVariation |
BEFREE |
To evaluate the association of genetic variants in genes involved in iron delivery and hepcidin regulation pathways with the risk of iron-deficiency anemia (IDA), the following single nucleotide polymorphisms were genotyped in 2139 unrelated elderly Chinese women: rs3811647 (TF), rs7385804 (TFR2), rs235756 (BMP2), and rs855791(V736A) and rs4820268 (TMPRSS6, encoding matriptase-2).
|
22323359 |
2012 |
|
rs3811647
|
|
|
0.010 |
GeneticVariation |
BEFREE |
To evaluate the association of genetic variants in genes involved in iron delivery and hepcidin regulation pathways with the risk of iron-deficiency anemia (IDA), the following single nucleotide polymorphisms were genotyped in 2139 unrelated elderly Chinese women: rs3811647 (TF), rs7385804 (TFR2), rs235756 (BMP2), and rs855791(V736A) and rs4820268 (TMPRSS6, encoding matriptase-2).
|
22323359 |
2012 |
|
rs4820268
|
|
|
0.010 |
GeneticVariation |
BEFREE |
To evaluate the association of genetic variants in genes involved in iron delivery and hepcidin regulation pathways with the risk of iron-deficiency anemia (IDA), the following single nucleotide polymorphisms were genotyped in 2139 unrelated elderly Chinese women: rs3811647 (TF), rs7385804 (TFR2), rs235756 (BMP2), and rs855791(V736A) and rs4820268 (TMPRSS6, encoding matriptase-2).
|
22323359 |
2012 |
|
rs7385804
|
|
|
0.010 |
GeneticVariation |
BEFREE |
To evaluate the association of genetic variants in genes involved in iron delivery and hepcidin regulation pathways with the risk of iron-deficiency anemia (IDA), the following single nucleotide polymorphisms were genotyped in 2139 unrelated elderly Chinese women: rs3811647 (TF), rs7385804 (TFR2), rs235756 (BMP2), and rs855791(V736A) and rs4820268 (TMPRSS6, encoding matriptase-2).
|
22323359 |
2012 |
|
rs1217691063
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The evaluation revealed mildly elevated homocysteine levels secondary to homozygous C677T alleles for MTHFR and iron deficiency anemia.
|
16814086 |
2006 |
|
rs1799899
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In menstruating white women, the G277S genotype was a risk factor for iron deficiency anaemia: iron deficiency anaemia was present in 27% of homozygous G277S/G277S women, 10% of G277G/G277S heterozygous women and 5% of homozygous wild-type G277G/G277G women.
|
11703331 |
2001 |