For example, Olazagoitia-Garmendia et al. have shown that allele-specific m6A (ASm6A) in lncRNAs, such as LOC339803, affects protein binding and chromatin localization, and that an SNP in the 5′UTR of XPO1 associated with celiac disease, which is close to three m6A consensus motifs (GGACT), exhibits higher m6A methylation, leading to increased XPO1 protein levels and activation of nuclear factor kappa B (NFkB), contributing to inflammation [27, 28]. Here, XPO1 is linked to celiac disease.