Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1217691063
rs1217691063
MTHFR
0.050 GeneticVariation BEFREE T/T genotype of MTHFR C677T polymorphism and C/C genotype of MTHFR A1298C are more likely to be associated with the susceptibility to NAFLD. 27128842

2016
dbSNP: rs1217691063
rs1217691063
MTHFR
0.050 GeneticVariation BEFREE By contrast, there was no significant difference in heterozygote MTHFR 677C/T and 1298A/C mutations, both MTHFR 677C/T and MTHFR 1298A/C mutations were more common in NAFLD groups compared with the control patients (p<0.001). 26031974

2015
dbSNP: rs1217691063
rs1217691063
MTHFR
0.050 GeneticVariation BEFREE No statistical difference for genotypes 677C/T (p = 0.110) and 1298A/C (p = 0.343) in patients with NAFLD and control subjects was observed. 23547829

2013
dbSNP: rs1217691063
rs1217691063
MTHFR
0.050 GeneticVariation BEFREE The MTHFR C677T and A1298C polymorphisms are not genetic risk factors for the development of NAFLD. 24051448

2013
dbSNP: rs1217691063
rs1217691063
MTHFR
0.050 GeneticVariation BEFREE According to this study, the MTHFR C677T mutation does not seem to be a risk factor for the progression of NAFL to NASH. 17356914

2007