Variant: rs1060499620

present in Gene: MECP2 present in Chromosome: X Position on Chromosome: 154030803 Alleles of this Variant: -/CT

rs1060499620 in MECP2 gene and Rett Syndrome PMID 23696494 2013 Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in Rett syndrome.