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rs2239464

From SNPedia

Orientationplus
Stabilizedplus
Make rs2239464(A;A)
Make rs2239464(A;G)
Make rs2239464(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154082978
GeneMECP2
is asnp
is mentioned by
dbSNPrs2239464
ebirs2239464
HLIrs2239464
Exacrs2239464
Varsomers2239464
Maprs2239464
PheGenIrs2239464
hapmaprs2239464
1000 genomesrs2239464
hgdprs2239464
ensemblrs2239464
gopubmedrs2239464
geneviewrs2239464
scholarrs2239464
googlers2239464
pharmgkbrs2239464
gwascentralrs2239464
openSNPrs2239464
23andMers2239464
23andMe allrs2239464
SNP Nexus

SNPshotrs2239464
SNPdbers2239464
MSV3drs2239464
GWAS Ctlgrs2239464
GMAF0.48
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 19717458OA-icon.png] A common MECP2 haplotype associates with reduced cortical surface area in humans in two independent populations.


[PMID 18320046OA-icon.png] Common variants within MECP2 confer risk of systemic lupus erythematosus.


[PMID 19333917OA-icon.png] 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