rs6701713
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6701713(A;A) |
Make rs6701713(A;G) |
Make rs6701713(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 207612944 |
Gene | CR1 |
is a | snp |
is | mentioned by |
dbSNP | rs6701713 |
dbSNP (classic) | rs6701713 |
ClinGen | rs6701713 |
ebi | rs6701713 |
HLI | rs6701713 |
Exac | rs6701713 |
Gnomad | rs6701713 |
Varsome | rs6701713 |
LitVar | rs6701713 |
Map | rs6701713 |
PheGenI | rs6701713 |
Biobank | rs6701713 |
1000 genomes | rs6701713 |
hgdp | rs6701713 |
ensembl | rs6701713 |
geneview | rs6701713 |
scholar | rs6701713 |
rs6701713 | |
pharmgkb | rs6701713 |
gwascentral | rs6701713 |
openSNP | rs6701713 |
23andMe | rs6701713 |
SNPshot | rs6701713 |
SNPdbe | rs6701713 |
MSV3d | rs6701713 |
GWAS Ctlg | rs6701713 |
GMAF | 0.2691 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 21460841] Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
[PMID 19734902] Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease.