rs6472155
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6472155(A;A) |
Make rs6472155(A;G) |
Make rs6472155(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 64817650 |
Gene | LOC105375878, LOC105375879 |
is a | snp |
is | mentioned by |
dbSNP | rs6472155 |
dbSNP (classic) | rs6472155 |
ClinGen | rs6472155 |
ebi | rs6472155 |
HLI | rs6472155 |
Exac | rs6472155 |
Gnomad | rs6472155 |
Varsome | rs6472155 |
LitVar | rs6472155 |
Map | rs6472155 |
PheGenI | rs6472155 |
Biobank | rs6472155 |
1000 genomes | rs6472155 |
hgdp | rs6472155 |
ensembl | rs6472155 |
geneview | rs6472155 |
scholar | rs6472155 |
rs6472155 | |
pharmgkb | rs6472155 |
gwascentral | rs6472155 |
openSNP | rs6472155 |
23andMe | rs6472155 |
SNPshot | rs6472155 |
SNPdbe | rs6472155 |
MSV3d | rs6472155 |
GWAS Ctlg | rs6472155 |
GMAF | 0.4233 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23393555![]() |
Trait | Retinopathy in non-diabetics |
Title | Genome-wide association study of retinopathy in individuals without diabetes. |
Risk Allele | A |
P-val | 4E-6 |
Odds Ratio | .23 [0.13-0.33] unit decrease |