rs3931397
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3931397(G;G) |
Make rs3931397(G;T) |
Make rs3931397(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 148158346 |
Gene | NR3C2 |
is a | snp |
is | mentioned by |
dbSNP | rs3931397 |
dbSNP (classic) | rs3931397 |
ClinGen | rs3931397 |
ebi | rs3931397 |
HLI | rs3931397 |
Exac | rs3931397 |
Gnomad | rs3931397 |
Varsome | rs3931397 |
LitVar | rs3931397 |
Map | rs3931397 |
PheGenI | rs3931397 |
Biobank | rs3931397 |
1000 genomes | rs3931397 |
hgdp | rs3931397 |
ensembl | rs3931397 |
geneview | rs3931397 |
scholar | rs3931397 |
rs3931397 | |
pharmgkb | rs3931397 |
gwascentral | rs3931397 |
openSNP | rs3931397 |
23andMe | rs3931397 |
SNPshot | rs3931397 |
SNPdbe | rs3931397 |
MSV3d | rs3931397 |
GWAS Ctlg | rs3931397 |
GMAF | 0.0978 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23291589] |
Trait | Corneal structure |
Title | Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus. |
Risk Allele | T |
P-val | 4E-8 |
Odds Ratio | .12 [0.061-0.179] unit decrease |