Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1448674651
rs1448674651
Entrez Id: 7298;55556
Gene Symbol: TYMS;ENOSF1
TYMS;ENOSF1
CUI: C0010068
Disease:
Coronary heart disease
0.010 GeneticVariation BEFREE Compound mutants for (MTHFD-G1958A, MTHFR-C677T and MTR-A2756G) and (MTHFD-G1958A, RFC1-G80A and MTR-A2756G) may increase the risk of CHD. 23701284 2013