Figure 2From: HERV-W polymorphism in chromosome X is associated with multiple sclerosis risk and with differential expression of MSRV Position of mapped amplicon in chromosome Xq22.3 (Ensembl Homo Sapiens version 66.37; March 2012) and schematic location of mutations (M1 and M2), insertion (Ins) and SNPs (rs6622139, rs6622140 and rs1290413), found in HERV-W region. Back to article page