Answers are grounded in this paper and cite their sources.
Our findings indicate that RA susceptibility is associated with multiple SNPs in MECP2 and IRAK1, but high linkage disequilibrium between them does not allow for further localization. Therefore, both genes remain candidates. Nevertheless, the major haplotype of the 2 nonsynonymous IRAK1 SNPs encoding for pPhe196Ser and pSer532Leu confers enhanced IRAK1 activity and, consequently, enhanced susceptibility to RA, as compared to the minor haplotype.
No takes yet. Share an insight, caveat, or question.
Han et al. (2012) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: