rs1979277, SHMT1

N. diseases: 45
Disease: Neural Tube Defects ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Neural Tube Defects
CUI: C0027794
Disease: Neural Tube Defects
0.030 GeneticVariation BEFREE The present study, using both case-control and family-based triad approach is the first report to demonstrate parental association of SHMT1 C1420T variant in conferring NTD risk in the fetus.Birth Defects Research, 2017.© 2017 Wiley Periodicals, Inc. 28411382 2017
Neural Tube Defects
CUI: C0027794
Disease: Neural Tube Defects
0.030 GeneticVariation BEFREE The present study, using both case-control and family-based triad approach is the first report to demonstrate parental association of SHMT1 C1420T variant in conferring NTD risk in the fetus. 28762673 2017
Neural Tube Defects
CUI: C0027794
Disease: Neural Tube Defects
0.030 GeneticVariation BEFREE Still, the influence of the 1420 C>T polymorphism of the cSHMT gene on the folate-related risk of NTD needs further investigation. 11386852 2001