[PMID 19717458] A common MECP2 haplotype associates with reduced cortical surface area in humans in two independent populations.


[PMID 18320046] Common variants within MECP2 confer risk of systemic lupus erythematosus.


[PMID 19333917] Variants within MECP2, a key transcription regulator, are associated with increased susceptibility to lupus and differential gene expression in patients with systemic lupus erythematosus.


[PMID 24043878] Common Variants on Xq28 Conferring Risk of Schizophrenia in Han Chinese


[PMID 23857988] Association of MeCP2 (rs2075596, rs2239464) genetic polymorphisms with systemic lupus erythematosus: a meta-analysis.


[PMID 25458699] Variants in IRAK1-MECP2 region confer susceptibility to autoimmune thyroid diseases

rs2239464

Parent Gene: MECP2

Importance: 1
Less common allele: G = 45%
More common allele: A = 55%
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