rs4938174
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4938174(A;A) |
Make rs4938174(A;G) |
Make rs4938174(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 111042516 |
is a | snp |
is | mentioned by |
dbSNP | rs4938174 |
dbSNP (classic) | rs4938174 |
ClinGen | rs4938174 |
ebi | rs4938174 |
HLI | rs4938174 |
Exac | rs4938174 |
Gnomad | rs4938174 |
Varsome | rs4938174 |
LitVar | rs4938174 |
Map | rs4938174 |
PheGenI | rs4938174 |
Biobank | rs4938174 |
1000 genomes | rs4938174 |
hgdp | rs4938174 |
ensembl | rs4938174 |
geneview | rs4938174 |
scholar | rs4938174 |
rs4938174 | |
pharmgkb | rs4938174 |
gwascentral | rs4938174 |
openSNP | rs4938174 |
23andMe | rs4938174 |
SNPshot | rs4938174 |
SNPdbe | rs4938174 |
MSV3d | rs4938174 |
GWAS Ctlg | rs4938174 |
GMAF | 0.259 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 | A |
P-val | 4E-9 |
Odds Ratio | .06 [0.04-0.08] unit increase |