Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397507444
rs397507444
MTHFR
0.020 GeneticVariation BEFREE Children with MTHFR C677T or A1298C polymorphisms who had normal neurological examination without a history of seizure were included in the study. 31734877

2020
dbSNP: rs397507444
rs397507444
MTHFR
0.020 GeneticVariation BEFREE Our study suggests that heterozygous variants of MTHFR (C677T and A1298C) gene are associated with poor seizure control in Pakhtun population of KP despite the fact that plasma level of carbamazepine were found within the therapeutic range. 30442198

2018