Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3761548
rs3761548
FOXP3
0.020 GeneticVariation BEFREE However, rs3761548 C allele was more prevalent in controls compared with patients with ACS (P = 0.024). 26931655

2016
dbSNP: rs3761548
rs3761548
FOXP3
0.020 GeneticVariation BEFREE In the present study, we analysed the expression of FOXP3 as well as the association between two variants in this gene (rs3761548A/C and rs5902434del/ATT) and occurrence of ACS in Iranian patients. 26931655

2016
dbSNP: rs3761548
rs3761548
FOXP3
0.020 GeneticVariation BEFREE Our results showed that single nucleotide polymorphism rs3761548 had association with ACS in Chinese Han population. 23299803

2013