rs2045084
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2045084(A;A) |
Make rs2045084(A;G) |
Make rs2045084(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 8 |
Position | 143611669 |
Gene | TSTA3 |
is a | snp |
is | mentioned by |
dbSNP | rs2045084 |
dbSNP (classic) | rs2045084 |
ClinGen | rs2045084 |
ebi | rs2045084 |
HLI | rs2045084 |
Exac | rs2045084 |
Gnomad | rs2045084 |
Varsome | rs2045084 |
LitVar | rs2045084 |
Map | rs2045084 |
PheGenI | rs2045084 |
Biobank | rs2045084 |
1000 genomes | rs2045084 |
hgdp | rs2045084 |
ensembl | rs2045084 |
geneview | rs2045084 |
scholar | rs2045084 |
rs2045084 | |
pharmgkb | rs2045084 |
gwascentral | rs2045084 |
openSNP | rs2045084 |
23andMe | rs2045084 |
SNPshot | rs2045084 |
SNPdbe | rs2045084 |
MSV3d | rs2045084 |
GWAS Ctlg | rs2045084 |
GMAF | 0.3613 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23585552] |
Trait | Rhegmatogenous retinal detachment |
Title | Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment. |
Risk Allele | G |
P-val | 3E-6 |
Odds Ratio | 1.16 [1.09-1.24] |