rs3850641 is a SNP in the TNFSF4 gene. It has been significantly associated with Myocardial infarction (MI).
''G'' allele could increase the susceptibility to breast cancer (P = 0.009662) [R].
''G'' allele is associated with lower serum high-density lipoprotein (HDL) cholesterol and apolipoprotein levels as compared to those of genotype AA [R].
The minor allele ''G'' was significantly more frequent in individuals with myocardial infarction than in controls [R].
The GG genotype was significantly associated with autoimmune thyroid diseases (AITDs). Moreover, the ''G'' allele was in strong association with hypothyroidism in Hashimoto's thyroiditis (HT) (p = 0.018) [R].