rs1877563
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1877563(A;A) |
Make rs1877563(A;G) |
Make rs1877563(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 39262973 |
Gene | LOC102724104 |
is a | snp |
is | mentioned by |
dbSNP | rs1877563 |
dbSNP (classic) | rs1877563 |
ClinGen | rs1877563 |
ebi | rs1877563 |
HLI | rs1877563 |
Exac | rs1877563 |
Gnomad | rs1877563 |
Varsome | rs1877563 |
LitVar | rs1877563 |
Map | rs1877563 |
PheGenI | rs1877563 |
Biobank | rs1877563 |
1000 genomes | rs1877563 |
hgdp | rs1877563 |
ensembl | rs1877563 |
geneview | rs1877563 |
scholar | rs1877563 |
rs1877563 | |
pharmgkb | rs1877563 |
gwascentral | rs1877563 |
openSNP | rs1877563 |
23andMe | rs1877563 |
SNPshot | rs1877563 |
SNPdbe | rs1877563 |
MSV3d | rs1877563 |
GWAS Ctlg | rs1877563 |
GMAF | 0.1336 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
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[PMID 24287500] Prospective Study of Common Variants in CX3CR1 and Risk of Macular Degeneration: Pooled Analysis From 5 Long-term Studies