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rs4938933

From SNPedia

Orientationplus
Stabilizedplus
Make rs4938933(C;C)
Make rs4938933(C;T)
Make rs4938933(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position60266956
is asnp
is mentioned by
dbSNPrs4938933
ebirs4938933
HLIrs4938933
Exacrs4938933
Varsomers4938933
Maprs4938933
PheGenIrs4938933
hapmaprs4938933
1000 genomesrs4938933
hgdprs4938933
ensemblrs4938933
gopubmedrs4938933
geneviewrs4938933
scholarrs4938933
googlers4938933
pharmgkbrs4938933
gwascentralrs4938933
openSNPrs4938933
23andMers4938933
23andMe allrs4938933
SNP Nexus

SNPshotrs4938933
SNPdbers4938933
MSV3drs4938933
GWAS Ctlgrs4938933
GMAF0.3705
Max Magnitude
? (C;C) (C;T) (T;T) 28
Alzheimer's disease associated, based on large 2011 study 10.1038/ng.801[PMID 21460841OA-icon.png] Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease


[PMID 26680604] Polygenic Analysis of Late-Onset Alzheimer's Disease from Mainland China.