rs1801394, FASTKD3;MTRR

N. diseases: 101
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 Moreover, the MTHFR C677T, MTHFR A1298C, and MTRR A66G polymorphisms were found to be significantly associated with the risk of certain subtypes of CTD. 30165839 2018