Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1217691063
rs1217691063
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.100 GeneticVariation BEFREE While MTHFR C677T and A1298C polymorphisms were not previously studied in an Arab population with respect to the susceptibility for developing schizophrenia, the MTRR A66G was not previously investigated in any population around the world. 22813657

2012

dbSNP: rs1217691063
rs1217691063
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.100 GeneticVariation BEFREE Overall, this study found no support that maternal/child MTHFR C677T genotype and maternal folate intake during pregnancy contribute to common aetiological pathways that are shared between schizophrenia and non-clinical psychotic symptoms in adolescents, assuming that decreased folate-status increases schizophrenia risk. 20418067

2010

dbSNP: rs1217691063
rs1217691063
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.100 GeneticVariation BEFREE The present findings suggest that the MTHFR C677T polymorphisms are likely to be associated with the risk of developing BD and schizophrenia and influence the age at onset of BD but not the age at onset of schizophrenia. 25101272

2014

dbSNP: rs1217691063
rs1217691063
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.100 GeneticVariation BEFREE MTHFR C677T genotype contributes to certain executive function deficits in schizophrenia. 17344026

2007

dbSNP: rs1217691063
rs1217691063
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.100 GeneticVariation BEFREE DNA methylation in schizophrenia subjects: gender and MTHFR 677C/T genotype differences. 22690662

2012

dbSNP: rs1217691063
rs1217691063
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.100 GeneticVariation BEFREE We carried out a meta-analysis of MTHFR C677T genotype and schizophrenia risk, and found that TT homozygotes had a significantly increased risk, OR 1.48 (1.18-1.86). 15729744

2005

dbSNP: rs1217691063
rs1217691063
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.100 GeneticVariation BEFREE We examined the prevalence of the catechol-O-methyltransferase (COMT) 324G>A (Val108/158Met) and methylenetetrahydrofolate reductase (MTHFR) 677C>T polymorphisms in 252 patients with schizophrenia and 405 control subjects.All subjects were of Dutch ancestry. 17716874

2008

dbSNP: rs1217691063
rs1217691063
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.100 GeneticVariation BEFREE Meta-analysis showed that MTHFR C677T was significantly associated with SZ, the highest OR was found for the recessive model (for TT vs. CT + CC: OR = 1.34, 95% CI: 1.18-1.53); a marginal association of MTHFR C677T with increased risk of BPD has also been found for the recessive model (OR = 1.26, 95% CI: 1.00-1.59). 24938371

2015

dbSNP: rs1217691063
rs1217691063
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.100 GeneticVariation BEFREE Transmission Disequilibrium Test (TDT) analysis showed no preferential transmission of the 677T allele from parents heterozygous for the MTHFR 677C > T polymorphism to schizophrenia offspring (P = 0.27). 17503473

2007

dbSNP: rs1217691063
rs1217691063
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.100 GeneticVariation BEFREE The aim was to detect a serum level of Hcy, examine the associations between the level of Hcy, methylenetetrahydrofolate reductase (MTHFR) gene C677T polymorphism and clinical properties for patients with schizophrenia, mood disorders and in a control group. 23586533

2014

dbSNP: rs1217691063
rs1217691063
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.100 GeneticVariation BEFREE A functional interaction between Catechol-O-Methyltransferase (COMT) Val158Met and methylenetetrahydrofolate reductase (MTHFR) C677T has been shown to differentially affect cognition in patients with schizophrenia and healthy controls; the effect of COMT Val158Met × MTHFR interaction on resilience to stress in patients and controls remains to be examined. 22128864

2012

dbSNP: rs1217691063
rs1217691063
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.100 GeneticVariation BEFREE The elevated risk of schizophrenia associated with the homozygous genotype of the MTHFR 677C>T polymorphism provides support for causality between a disturbed homocysteine metabolism and risk of schizophrenia. 16172608

2006

dbSNP: rs1217691063
rs1217691063
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.100 GeneticVariation BEFREE The MTHFR C677T polymorphism may play a role as a modifying factor for age of onset in schizophrenia. 19746410

2010

dbSNP: rs1217691063
rs1217691063
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.100 GeneticVariation BEFREE Homozygosity for MTHFR C677T was associated with higher tHcy concentrations in control and schizophrenia groups (P<0.01), which was mainly driven by the male group. 16076517

2005

dbSNP: rs1217691063
rs1217691063
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.100 GeneticVariation BEFREE Association study of methylenetetrahydrofolate reductase genetic polymorphism 677C>T with schizophrenia in hospitalized patients in population of European Russia. 29202425

2018

dbSNP: rs1217691063
rs1217691063
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.100 GeneticVariation BEFREE MTHFR C677T and COMT Val158Met interact with CA to increase risk of schizophrenia. 28556887

2017

dbSNP: rs1217691063
rs1217691063
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.100 GeneticVariation BEFREE While C677T is known to play major roles in the risk of adult schizophrenia, our finding for the first time suggests an age-specific association between MTHFR polymorphisms and schizophrenia. 31302825

2019

dbSNP: rs1217691063
rs1217691063
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.100 GeneticVariation BEFREE However, neither the MTHFR C677T nor the A1298C polymorphisms are associated with schizophrenia in women. 16084002

2005

dbSNP: rs1217691063
rs1217691063
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.100 GeneticVariation BEFREE A hypomethylating variant of MTHFR, 677C>T, blunts the neural response to errors in patients with schizophrenia and healthy individuals. 21980405

2011

dbSNP: rs1217691063
rs1217691063
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.100 GeneticVariation BEFREE We investigated a possible interaction between MTHFR 677C>T polymorphism and winter birth in the development of schizophrenia in a group of 742 schizophrenia patients and 884 control subjects.All subjects were of Dutch ancestry. 21093223

2011

dbSNP: rs1217691063
rs1217691063
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.100 GeneticVariation BEFREE The T-allele of the C677T polymorphism has recently been associated with earlier age at onset of schizophrenia. 21302350

2011

dbSNP: rs1217691063
rs1217691063
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.100 GeneticVariation BEFREE In conclusion, both elevated plasma homocysteine levels and variation in the MTHFR 677C-->T gene are related to increased rates of schizophrenia and are risk factors for schizophrenia. 19564051

2009

dbSNP: rs1217691063
rs1217691063
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.100 GeneticVariation BEFREE Elevated Hcy levels and, in line with this finding, homozygosity for the 677C-->T mutation in the MTHFR gene were not associated with an increased risk for schizophrenia. 14572619

2003

dbSNP: rs1217691063
rs1217691063
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.100 GeneticVariation BEFREE These results do not support a role for the C677T MTHFR variant in schizophrenia. 16969279

2006

dbSNP: rs1217691063
rs1217691063
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.100 GeneticVariation BEFREE In conclusion the results of the present meta-analysis suggested that the MTHFR C677T polymorphism is a ris</span>k factor for schizophrenia</span>. 27025471

2016