rs2669845
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2669845(C;C) |
Make rs2669845(C;T) |
Make rs2669845(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 39279727 |
Gene | CX3CR1 |
is a | snp |
is | mentioned by |
dbSNP | rs2669845 |
dbSNP (classic) | rs2669845 |
ClinGen | rs2669845 |
ebi | rs2669845 |
HLI | rs2669845 |
Exac | rs2669845 |
Gnomad | rs2669845 |
Varsome | rs2669845 |
LitVar | rs2669845 |
Map | rs2669845 |
PheGenI | rs2669845 |
Biobank | rs2669845 |
1000 genomes | rs2669845 |
hgdp | rs2669845 |
ensembl | rs2669845 |
geneview | rs2669845 |
scholar | rs2669845 |
rs2669845 | |
pharmgkb | rs2669845 |
gwascentral | rs2669845 |
openSNP | rs2669845 |
23andMe | rs2669845 |
SNPshot | rs2669845 |
SNPdbe | rs2669845 |
MSV3d | rs2669845 |
GWAS Ctlg | rs2669845 |
GMAF | 0.1074 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 24287500] Prospective Study of Common Variants in CX3CR1 and Risk of Macular Degeneration: Pooled Analysis From 5 Long-term Studies