Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137853061
rs137853061
Entrez Id: 4552
Gene Symbol: MTRR
MTRR
CUI: C1856057
Disease:
Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type
0.800 GeneticVariation UNIPROT Molecular basis for methionine synthase reductase deficiency in patients belonging to the cblE complementation group of disorders in folatecobalamin metabolism. 10484769 1999
dbSNP: rs137853061
rs137853061
Entrez Id: 4552
Gene Symbol: MTRR
MTRR
CUI: C1856057
Disease:
Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type
0.800 GeneticVariation UNIPROT Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuria. 9501215 1998
dbSNP: rs137853061
rs137853061
Entrez Id: 4552
Gene Symbol: MTRR
MTRR
CUI: C1856057
Disease:
Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type
A 0.800 CausalMutation CLINVAR
dbSNP: rs7721678
rs7721678
Entrez Id: 4552
Gene Symbol: MTRR
MTRR
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs768980918
rs768980918
Entrez Id: 4552
Gene Symbol: MTRR
MTRR
CUI: C1856057
Disease:
Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type
T 0.700 CausalMutation CLINVAR Clinical onset and course, response to treatment and outcome in 24 patients with the cblE or cblG remethylation defect complemented by genetic and in vitro enzyme study data. 25526710 2015
dbSNP: rs761061866
rs761061866
Entrez Id: 4552
Gene Symbol: MTRR
MTRR
CUI: C1856057
Disease:
Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type
0.700 GeneticVariation UNIPROT Molecular basis for methionine synthase reductase deficiency in patients belonging to the cblE complementation group of disorders in folatecobalamin metabolism. 10484769 1999
dbSNP: rs761061866
rs761061866
Entrez Id: 4552
Gene Symbol: MTRR
MTRR
CUI: C1856057
Disease:
Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type
0.700 GeneticVariation UNIPROT Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuria. 9501215 1998
dbSNP: rs768980918
rs768980918
Entrez Id: 4552
Gene Symbol: MTRR
MTRR
CUI: C1856057
Disease:
Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type
T 0.700 CausalMutation CLINVAR Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuria. 9501215 1998
dbSNP: rs137853062
rs137853062
Entrez Id: 4552
Gene Symbol: MTRR
MTRR
CUI: C1856057
Disease:
Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type
T 0.700 CausalMutation CLINVAR
dbSNP: rs1554006017
rs1554006017
Entrez Id: 4552
Gene Symbol: MTRR
MTRR
CUI: C1856057
Disease:
Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type
G 0.700 CausalMutation CLINVAR
dbSNP: rs1801394
rs1801394
Entrez Id: 4552;79072
Gene Symbol: MTRR;FASTKD3
MTRR;FASTKD3
CUI: C0027794
Disease:
Neural Tube Defects
0.100 GeneticVariation BEFREE MTHFR (C677T, A1298C) and MTRR A66G polymorphisms were found to be protector factors for NTD fetuses in the mother group. 31238314 2019
dbSNP: rs1801394
rs1801394
Entrez Id: 4552;79072
Gene Symbol: MTRR;FASTKD3
MTRR;FASTKD3
CUI: C0010068
Disease:
Coronary heart disease
0.100 GeneticVariation BEFREE Our overall analyses suggested that <i>MTRR</i> rs1801394, <i>MTRR</i> rs1532268, <i>MTHFR</i> rs1801131 and <i>MTHFR</i> rs1801133 polymorphisms were all significantly associated with the risk of CHD in certain genetic models. 30333252 2018
dbSNP: rs1801394
rs1801394
Entrez Id: 4552;79072
Gene Symbol: MTRR;FASTKD3
MTRR;FASTKD3
CUI: C0027794
Disease:
Neural Tube Defects
0.100 GeneticVariation BEFREE Our results suggest that rs2236225 of MTHFD1 gene, rs1801133 of MTHFR gene and rs1801394 of MTRR gene were associated with NTDs in Han population of Northern China. 29392422 2018
dbSNP: rs1801394
rs1801394
Entrez Id: 4552;79072
Gene Symbol: MTRR;FASTKD3
MTRR;FASTKD3
CUI: C0013080
Disease:
Down Syndrome
0.100 GeneticVariation BEFREE The study aim to investigate MTHFR C677T, MTHFR A1298C, RFC1 A80G, MTR A2756G, CBS 844ins68, MTRR A66G polymorphisms in Down syndrome (DS) parents. 29130768 2017
dbSNP: rs1801394
rs1801394
Entrez Id: 4552;79072
Gene Symbol: MTRR;FASTKD3
MTRR;FASTKD3
CUI: C0010068
Disease:
Coronary heart disease
0.100 GeneticVariation BEFREE Also, MTRR A66G and C524T polymorphisms were associated with a higher CHD risk in the homozygote comparison of wild and mutant genotypes and also in heterozygote and mutant comparison. 28778621 2017
dbSNP: rs1801394
rs1801394
Entrez Id: 4552;79072
Gene Symbol: MTRR;FASTKD3
MTRR;FASTKD3
CUI: C4521042
Disease:
Complete Trisomy 21 Syndrome
0.100 GeneticVariation BEFREE The study aim to investigate MTHFR C677T, MTHFR A1298C, RFC1 A80G, MTR A2756G, CBS 844ins68, MTRR A66G polymorphisms in Down syndrome (DS) parents. 29130768 2017
dbSNP: rs1801394
rs1801394
Entrez Id: 4552;79072
Gene Symbol: MTRR;FASTKD3
MTRR;FASTKD3
CUI: C0027794
Disease:
Neural Tube Defects
0.100 GeneticVariation BEFREE Overall, we found that maternal MTHFR C677T polymorphism (OR(TvsC) =1.20; 95% CI = 1.13-1.28) and MTRR A66G polymorphism (OR(GvsA) = 1.21; 95% CI = 0.98-1.49) were risk factors for producing offspring with NTD but maternal MTHFR A1298C polymorphism (OR(CvsA) = 0.91; 95% CI = 0.78-1.07) was not associated with NTD risk. 25005003 2015
dbSNP: rs1801394
rs1801394
Entrez Id: 4552;79072
Gene Symbol: MTRR;FASTKD3
MTRR;FASTKD3
CUI: C0027794
Disease:
Neural Tube Defects
0.100 GeneticVariation BEFREE The further meta-analysis enhance that MTRR 66A>G was connected with the susceptibility of NTDs widely. 26334892 2015
dbSNP: rs1801394
rs1801394
Entrez Id: 4552;79072
Gene Symbol: MTRR;FASTKD3
MTRR;FASTKD3
CUI: C4521042
Disease:
Complete Trisomy 21 Syndrome
0.100 GeneticVariation BEFREE There was evidence for an association between the MTRR c.66A>G</span> (rs1801394) polymorphism and maternal risk for DS. 25544792 2014
dbSNP: rs1801394
rs1801394
Entrez Id: 4552;79072
Gene Symbol: MTRR;FASTKD3
MTRR;FASTKD3
CUI: C0013080
Disease:
Down Syndrome
0.100 GeneticVariation BEFREE There was evidence for an association between the MTRR c.66A>G</span> (rs1801394) polymorphism and maternal risk for DS. 25544792 2014
dbSNP: rs1801394
rs1801394
Entrez Id: 4552;79072
Gene Symbol: MTRR;FASTKD3
MTRR;FASTKD3
CUI: C0013080
Disease:
Down Syndrome
0.100 GeneticVariation BEFREE Overall, present data suggest that the MTRR c.66A>G polymorphism represents a risk factor for the birth of a child with DS among white Caucasian women. 24965145 2014
dbSNP: rs1801394
rs1801394
Entrez Id: 4552;79072
Gene Symbol: MTRR;FASTKD3
MTRR;FASTKD3
CUI: C4521042
Disease:
Complete Trisomy 21 Syndrome
0.100 GeneticVariation BEFREE Overall, present data suggest that the MTRR c.66A>G polymorphism represents a risk factor for the birth of a child with DS among white Caucasian women. 24965145 2014
dbSNP: rs1801394
rs1801394
Entrez Id: 4552;79072
Gene Symbol: MTRR;FASTKD3
MTRR;FASTKD3
CUI: C0010068
Disease:
Coronary heart disease
0.100 GeneticVariation BEFREE Evidence is mounting for the association between MTRR A66G (rs1801394)/MTR A2756G (rs1805087) and the CHD risk, but results are controversial. 24595101 2014
dbSNP: rs1801394
rs1801394
Entrez Id: 4552;79072
Gene Symbol: MTRR;FASTKD3
MTRR;FASTKD3
CUI: C0010068
Disease:
Coronary heart disease
0.100 GeneticVariation BEFREE The results showed that MTRR A66G polymorphism was associated with a higher CHD risk in the allele comparison (G vs A: OR 1.163; 95 % CI 1.016-1.330; P heterogeneity = 0.004), the homozygote comparison (GG vs AA: OR 1.332; 95 % CI 1.020-1.740; P heterogeneity = 0.035), and the dominant model (GG/AG vs AA: OR 1.218; 95 % CI 1.001-1.482; P heterogeneity = 0.001). 24913415 2014
dbSNP: rs1801394
rs1801394
Entrez Id: 4552;79072
Gene Symbol: MTRR;FASTKD3
MTRR;FASTKD3
CUI: C0013080
Disease:
Down Syndrome
0.100 GeneticVariation BEFREE This meta-analysis indicates that maternal MTRR 66A>G polymorphism is associated with an increased risk of having a DS child. 23094987 2013