rs775144154, SLC19A1

N. diseases: 38
Disease: Conotruncal defect ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Conotruncal defect
CUI: C1853238
Disease: Conotruncal defect
0.010 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