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rs2573905

From SNPedia

Orientationplus
Stabilizedplus
Make rs2573905(C;C)
Make rs2573905(C;T)
Make rs2573905(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position92147221
GenePCDH11X
is asnp
is mentioned by
dbSNPrs2573905
ebirs2573905
HLIrs2573905
Exacrs2573905
Varsomers2573905
Maprs2573905
PheGenIrs2573905
hapmaprs2573905
1000 genomesrs2573905
hgdprs2573905
ensemblrs2573905
gopubmedrs2573905
geneviewrs2573905
scholarrs2573905
googlers2573905
pharmgkbrs2573905
gwascentralrs2573905
openSNPrs2573905
23andMers2573905
23andMe allrs2573905
SNP Nexus

SNPshotrs2573905
SNPdbers2573905
MSV3drs2573905
GWAS Ctlgrs2573905
GMAF0.3881
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19136949OA-icon.png]
Trait Alzheimer's disease
Title Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease
Risk Allele
P-val 2E-7
Odds Ratio 1.29 [1.17-1.42]



[PMID 20523261OA-icon.png] PCDH11X variation is not associated with late-onset Alzheimer disease susceptibility


GET Evidence
rs2573905
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.445652
summary