rs2509897
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2509897(C;C) |
Make rs2509897(C;G) |
Make rs2509897(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 57595144 |
is a | snp |
is | mentioned by |
dbSNP | rs2509897 |
dbSNP (classic) | rs2509897 |
ClinGen | rs2509897 |
ebi | rs2509897 |
HLI | rs2509897 |
Exac | rs2509897 |
Gnomad | rs2509897 |
Varsome | rs2509897 |
LitVar | rs2509897 |
Map | rs2509897 |
PheGenI | rs2509897 |
Biobank | rs2509897 |
1000 genomes | rs2509897 |
hgdp | rs2509897 |
ensembl | rs2509897 |
geneview | rs2509897 |
scholar | rs2509897 |
rs2509897 | |
pharmgkb | rs2509897 |
gwascentral | rs2509897 |
openSNP | rs2509897 |
23andMe | rs2509897 |
SNPshot | rs2509897 |
SNPdbe | rs2509897 |
MSV3d | rs2509897 |
GWAS Ctlg | rs2509897 |
GMAF | 0.2222 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 20161815] SERPING1 polymorphisms in polypoidal choroidal vasculopathy
[PMID 19169411] Common variation in the SERPING1 gene is not associated with age-related macular degeneration in two independent groups of subjects.