Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397507444
rs397507444
0.040 GeneticVariation BEFREE Our findings suggest a strong association between maternal MTHFR A1298C and risk of TS in Egypt. 26217949

2015

dbSNP: rs397507444
rs397507444
0.040 GeneticVariation BEFREE The polymorphisms MTHFR 677C>T and 1298A>C, MTR 2756A>G, RFC1 80G>A, and TYMS 2R/3R-alone or in combinations-were not associated with the risk of chromosomal aneuploidy in TS. 25858821

2015

dbSNP: rs397507444
rs397507444
0.040 GeneticVariation BEFREE The results suggest that the C677T and A1298C polymorphisms of the MTHFR gene are not related to homocysteine levels in Brazilian patients with TS, despite the differential distribution of the mutated allele C (A1298C) in these patients. 22283972

2012

dbSNP: rs397507444
rs397507444
0.040 GeneticVariation BEFREE As for polymorphism A1298C, the patients with Turner Syndrome and chromosome mosaicism presented genotypes 1298AA, 1298AC and 1298CC at the following frequencies: 58.3%, 27.8% and 13.9%, respectively. 19169497

2008