rs4938933
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4938933(C;C) |
Make rs4938933(C;T) |
Make rs4938933(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 60266956 |
is a | snp |
is | mentioned by |
dbSNP | rs4938933 |
dbSNP (classic) | rs4938933 |
ClinGen | rs4938933 |
ebi | rs4938933 |
HLI | rs4938933 |
Exac | rs4938933 |
Gnomad | rs4938933 |
Varsome | rs4938933 |
LitVar | rs4938933 |
Map | rs4938933 |
PheGenI | rs4938933 |
Biobank | rs4938933 |
1000 genomes | rs4938933 |
hgdp | rs4938933 |
ensembl | rs4938933 |
geneview | rs4938933 |
scholar | rs4938933 |
rs4938933 | |
pharmgkb | rs4938933 |
gwascentral | rs4938933 |
openSNP | rs4938933 |
23andMe | rs4938933 |
SNPshot | rs4938933 |
SNPdbe | rs4938933 |
MSV3d | rs4938933 |
GWAS Ctlg | rs4938933 |
GMAF | 0.3705 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
Alzheimer's disease associated, based on large 2011 study 10.1038/ng.801
[PMID 21460841] 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.