Have questions? Visit https://www.reddit.com/r/SNPedia

rs4568761

From SNPedia

Orientationplus
Stabilizedplus
Make rs4568761(C;C)
Make rs4568761(C;T)
Make rs4568761(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position92184068
GenePCDH11X
is asnp
is mentioned by
dbSNPrs4568761
dbSNP (old)rs4568761
ClinGenrs4568761
ebirs4568761
HLIrs4568761
Exacrs4568761
Gnomadrs4568761
Varsomers4568761
Maprs4568761
PheGenIrs4568761
Biobankrs4568761
1000 genomesrs4568761
hgdprs4568761
ensemblrs4568761
gopubmedrs4568761
geneviewrs4568761
scholarrs4568761
googlers4568761
pharmgkbrs4568761
gwascentralrs4568761
openSNPrs4568761
23andMers4568761
23andMe allrs4568761
SNP Nexus

SNPshotrs4568761
SNPdbers4568761
MSV3drs4568761
GWAS Ctlgrs4568761
GMAF0.3077
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.