rs116806486
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs116806486(A;A) |
Make rs116806486(A;G) |
Make rs116806486(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 207523640 |
Gene | CR1 |
is a | snp |
is | mentioned by |
dbSNP | rs116806486 |
dbSNP (classic) | rs116806486 |
ClinGen | rs116806486 |
ebi | rs116806486 |
HLI | rs116806486 |
Exac | rs116806486 |
Gnomad | rs116806486 |
Varsome | rs116806486 |
LitVar | rs116806486 |
Map | rs116806486 |
PheGenI | rs116806486 |
Biobank | rs116806486 |
1000 genomes | rs116806486 |
hgdp | rs116806486 |
ensembl | rs116806486 |
geneview | rs116806486 |
scholar | rs116806486 |
rs116806486 | |
pharmgkb | rs116806486 |
gwascentral | rs116806486 |
openSNP | rs116806486 |
23andMe | rs116806486 |
SNPshot | rs116806486 |
SNPdbe | rs116806486 |
MSV3d | rs116806486 |
GWAS Ctlg | rs116806486 |
GMAF | 0.002755 |
Max Magnitude | 0 |
[PMID 24018213] Missense variants in CR1 are associated with increased risk of Alzheimer' disease in Han Chinese