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rs2734647

From SNPedia

Orientationplus
Stabilizedplus
Make rs2734647(C;C)
Make rs2734647(C;T)
Make rs2734647(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154026729
GeneMeCP2, MECP2
is asnp
is mentioned by
dbSNPrs2734647
ebirs2734647
HLIrs2734647
Exacrs2734647
Varsomers2734647
Maprs2734647
PheGenIrs2734647
hapmaprs2734647
1000 genomesrs2734647
hgdprs2734647
ensemblrs2734647
gopubmedrs2734647
geneviewrs2734647
scholarrs2734647
googlers2734647
pharmgkbrs2734647
gwascentralrs2734647
openSNPrs2734647
23andMers2734647
23andMe allrs2734647
SNP Nexus

SNPshotrs2734647
SNPdbers2734647
MSV3drs2734647
GWAS Ctlgrs2734647
GMAF0.3277
Max Magnitude
? (C;C) (C;T) (T;T) 28

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


[PMID 18454203OA-icon.png] Differential allelic expression in the human genome: a robust approach to identify genetic and epigenetic cis-acting mechanisms regulating gene expression.