Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397507444
rs397507444
MTHFR
0.030 GeneticVariation BEFREE Subjects carrying both variant genotypes of MTHFR A1298C and SLC19A1 G80A had a higher (3.23 [1.71-6.02], p = 0.0002) increased risk for CTDs. 30165839

2018
dbSNP: rs397507444
rs397507444
MTHFR
0.030 GeneticVariation BEFREE The A1298C Methylenetetrahydrofolate Reductase Gene Variant as a Susceptibility Gene for Non-Syndromic Conotruncal Heart Defects in an Indian Population. 25981563

2015
dbSNP: rs397507444
rs397507444
MTHFR
0.030 GeneticVariation BEFREE Association between 5,10-methylenetetrahydrofolate reductase C677T and A1298C polymorphisms and conotruncal heart defects. 12705333

2003