Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1217691063
rs1217691063
0.050 GeneticVariation BEFREE The aim of this study was to examine the association between MTHFR C677T genotype and IBD in the different Jewish populations.DNA samples were assessed for the presence of the MTHFR C677T variant allele in 445 Jewish Israeli IBD patients: 338 with Crohn's disease [CD] (214 Ashkenazi and 124 non-Ashkenazi Jews) and 107 with ulcerative colitis [UC] (73 Ashkenazi and 34 non-Ashkenazi Jews), and in 347 healthy controls: 173 Ashkenazi and 174 Non-Ashkenazi Jews. 28002332

2016

dbSNP: rs1217691063
rs1217691063
0.050 GeneticVariation BEFREE Methylenetetrahydrofolate reductase C677T variant in Moroccan patients with inflammatory bowel disease. 23542077

2013

dbSNP: rs1217691063
rs1217691063
0.050 GeneticVariation BEFREE Deficient folate status is associated with a higher impact of MTHFR C677T polymorphism on IBD risk. 21967576

2011

dbSNP: rs1217691063
rs1217691063
0.050 GeneticVariation BEFREE Hyperhomocysteinemia and methylenetetrahydrofolate reductase 677C-->T and 1298A-->C mutations in patients with inflammatory bowel disease. 16262529

2005

dbSNP: rs1217691063
rs1217691063
0.050 GeneticVariation BEFREE There is an association between the thermolabile MTHFR C677T variant and IBD. 10446107

1999