rs12676170
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12676170(A;A) |
Make rs12676170(A;G) |
Make rs12676170(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 15339908 |
is a | snp |
is | mentioned by |
dbSNP | rs12676170 |
dbSNP (classic) | rs12676170 |
ClinGen | rs12676170 |
ebi | rs12676170 |
HLI | rs12676170 |
Exac | rs12676170 |
Gnomad | rs12676170 |
Varsome | rs12676170 |
LitVar | rs12676170 |
Map | rs12676170 |
PheGenI | rs12676170 |
Biobank | rs12676170 |
1000 genomes | rs12676170 |
hgdp | rs12676170 |
ensembl | rs12676170 |
geneview | rs12676170 |
scholar | rs12676170 |
rs12676170 | |
pharmgkb | rs12676170 |
gwascentral | rs12676170 |
openSNP | rs12676170 |
23andMe | rs12676170 |
SNPshot | rs12676170 |
SNPdbe | rs12676170 |
MSV3d | rs12676170 |
GWAS Ctlg | rs12676170 |
GMAF | 0.2525 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23322567] |
Trait | Corneal astigmatism |
Title | Identification of a candidate gene for astigmatism. |
Risk Allele | A |
P-val | 8E-6 |
Odds Ratio | .05 [NR] unit decrease |