rs2239464

Orientation

plus

Stabilized

plus

Make rs2239464(A;A)

Make rs2239464(A;G)

Make rs2239464(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

154082978

Gene

MECP2

is a	snp
is	mentioned by
dbSNP	rs2239464
dbSNP (classic)	rs2239464
ClinGen	rs2239464
ebi	rs2239464
HLI	rs2239464
Exac	rs2239464
Gnomad	rs2239464
Varsome	rs2239464
LitVar	rs2239464
Map	rs2239464
PheGenI	rs2239464
Biobank	rs2239464
1000 genomes	rs2239464
hgdp	rs2239464
ensembl	rs2239464
geneview	rs2239464
scholar	rs2239464
google	rs2239464
pharmgkb	rs2239464
gwascentral	rs2239464
openSNP	rs2239464
23andMe	rs2239464
SNPshot	rs2239464
SNPdbe	rs2239464
MSV3d	rs2239464
GWAS Ctlg	rs2239464

GMAF

0.48

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

[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