Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3761548
rs3761548
FOXP3
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.040 GeneticVariation BEFREE The aim of this study was to evaluate the association between rs3761548 FOXP3 (-3279 C > A) variant and multiple sclerosis (MS), disability, disability progression, as well as transforming growth factor (TGF)-β1 and interleukin (IL)-10 plasma levels in MS patients. 31414141

2019
dbSNP: rs3761548
rs3761548
FOXP3
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.040 GeneticVariation BEFREE FOXP3 gene polymorphism rs3761548 was associated with a higher MS risk, especially in Asians. 31567981

2019
dbSNP: rs3761548
rs3761548
FOXP3
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.040 GeneticVariation BEFREE The purpose of our study was to evaluate the association of chosen polymorphisms of FOXP3 gene (rs3761549, rs3761548, rs3761547) with different clinical multiple sclerosis (MS) data of our relapsing-remitting groups of patients and in control group. 30229436

2018
dbSNP: rs3761548
rs3761548
FOXP3
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.040 GeneticVariation BEFREE The frequencies of AA and AC genotypes at rs3761548 in the FOXP3 gene were significantly higher in MS group as compared with healthy subjects (P < 0.05). 25326790

2015