Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1217691063
rs1217691063
0.070 GeneticVariation BEFREE Relationship between genetic polymorphisms MTHFR (C677T, A1298C), MTR (A2756G) and MTRR (A66G) genes and multiple sclerosis: a case-control study. 31038186

2019

dbSNP: rs1217691063
rs1217691063
0.070 GeneticVariation BEFREE We performed a meta-analysis on the association between MS and the following genotypes: MTHFR C677T, A1298C, and GSTP1 A313G polymorphisms, and GSTM1 and GSTT1 null alleles. 26150166

2015

dbSNP: rs1217691063
rs1217691063
0.070 GeneticVariation BEFREE These results showed that T allele of C677T polymorphism was associated with MS susceptibility in Turkish population. 25203152

2014

dbSNP: rs1217691063
rs1217691063
0.070 GeneticVariation BEFREE Although our preliminary findings suggest no association between the MTHFR C677T variants and MS, there is evidence to suggest a significant association between the MTHFR A1298C polymorphisms and MS. 23523621

2013

dbSNP: rs1217691063
rs1217691063
0.070 GeneticVariation BEFREE We concluded that having T allele of C677T in MS might be accompanied with higher levels of serum inflammatory mediators and a vulnerability to earlier age of onset of disease. 21190091

2011

dbSNP: rs1217691063
rs1217691063
0.070 GeneticVariation BEFREE MTHFR c.677C>T (p.A222V) and c.1298A>C (p.E429A), in 138 patients with clinically definite multiple sclerosis of relapsing-remitting course and 138 age- and gender-matched healthy controls. 19854238

2010

dbSNP: rs1217691063
rs1217691063
0.070 GeneticVariation BEFREE Thus, the C677T mutation of the MTHFR gene may influence MS susceptibility. 16564429

2006