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rs5941047

From SNPedia

Orientationplus
Stabilizedplus
Make rs5941047(C;C)
Make rs5941047(C;T)
Make rs5941047(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position92176386
GenePCDH11X
is asnp
is mentioned by
dbSNPrs5941047
ebirs5941047
HLIrs5941047
Exacrs5941047
Varsomers5941047
Maprs5941047
PheGenIrs5941047
hapmaprs5941047
1000 genomesrs5941047
hgdprs5941047
ensemblrs5941047
gopubmedrs5941047
geneviewrs5941047
scholarrs5941047
googlers5941047
pharmgkbrs5941047
gwascentralrs5941047
openSNPrs5941047
23andMers5941047
23andMe allrs5941047
SNP Nexus

SNPshotrs5941047
SNPdbers5941047
MSV3drs5941047
GWAS Ctlgrs5941047
GMAF0.4849
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 20523261OA-icon.png] PCDH11X variation is not associated with late-onset Alzheimer disease susceptibility


[PMID 19136949OA-icon.png] Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease.