Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3850641
rs3850641
TNFSF4
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome 		0.020 GeneticVariation BEFREE When we stratified eligible studies by type of disease, positive results were observed for rs17568 variant in subjects with acute coronary syndrome (ACS) (allele model: P = 0.04, OR = 0.81, 95%CI, 0.65-0.99), for rs1234314 variant in subjects with coronary artery disease (CAD) (dominant model: P = 0.04, OR = 1.16, 95%CI, 1.00-1.35), for rs3850641 variant in subjects with CAD (recessive model: P = 0.02, OR = 1.42, 95%CI, 1.05-1.90) and myocardial infarction (MI) (recessive model: P = 0.03, OR = 1.49, 95%CI, 1.05-2.11). 30614039

2019
dbSNP: rs3850641
rs3850641
TNFSF4
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome 		0.020 GeneticVariation BEFREE No significant association between rs2298212A/G or rs3850641A/G and the risk of ACS was found in this study. 21476935

2011