Disease: Myocardial Infarction ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6922269
rs6922269
Entrez Id: 25902
Gene Symbol: MTHFD1L
MTHFD1L
CUI: C0027051
Disease:
Myocardial Infarction 		0.040 GeneticVariation BEFREE One of them is the marker rs6922269, which has been suggested as a risk factor for development of MI in Western populations. 25809277 2015
dbSNP: rs6922269
rs6922269
Entrez Id: 25902
Gene Symbol: MTHFD1L
MTHFD1L
CUI: C0027051
Disease:
Myocardial Infarction 		0.040 GeneticVariation BEFREE No association for MI or lipid levels was found for SNPs rs2943634 and rs6922269 (P-adj > 0.05). 21463265 2011
dbSNP: rs6922269
rs6922269
Entrez Id: 25902
Gene Symbol: MTHFD1L
MTHFD1L
CUI: C0027051
Disease:
Myocardial Infarction 		0.040 GeneticVariation BEFREE One marker, rs6922269, in MTHFD1L was significantly protective against MI (OR=0.68, p=0.0035), while the variant rs4977574 in CDKN2A-CDKN2B was significantly associated with MI (OR=1.33, p=0.0086). 22216278 2011
dbSNP: rs6922269
rs6922269
Entrez Id: 25902
Gene Symbol: MTHFD1L
MTHFD1L
CUI: C0027051
Disease:
Myocardial Infarction 		0.040 GeneticVariation BEFREE The aim of the present case-control study including 324 healthy controls and 296 patients with coronary heart disease from Tunisia, was to assess relation between three polymorphisms previously reported to be strongly associated with coronary heart disease in the Welcome Trust Case Control Consortium (WTCCC) and the German myocardial infarction family studies: locus 9p21.3 (rs 1333049), locus 6q25.1 (rs6922269) and 2q36.3 (rs2943634). 19373437 2010