rs2721051
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common on affy axiom data |
| Make rs2721051(A;A) |
| Make rs2721051(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 40536747 |
| Gene | LOC100289058 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2721051 |
| dbSNP (classic) | rs2721051 |
| ClinGen | rs2721051 |
| ebi | rs2721051 |
| HLI | rs2721051 |
| Exac | rs2721051 |
| Gnomad | rs2721051 |
| Varsome | rs2721051 |
| LitVar | rs2721051 |
| Map | rs2721051 |
| PheGenI | rs2721051 |
| Biobank | rs2721051 |
| 1000 genomes | rs2721051 |
| hgdp | rs2721051 |
| ensembl | rs2721051 |
| geneview | rs2721051 |
| scholar | rs2721051 |
| rs2721051 | |
| pharmgkb | rs2721051 |
| gwascentral | rs2721051 |
| openSNP | rs2721051 |
| 23andMe | rs2721051 |
| SNPshot | rs2721051 |
| SNPdbe | rs2721051 |
| MSV3d | rs2721051 |
| GWAS Ctlg | rs2721051 |
| GMAF | 0.07713 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20485516 ]
|
| Trait | Central corneal thickness |
| Title | Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness |
| Risk Allele | G |
| P-val | 5E-10 |
| Odds Ratio | 0.24 [0.16-0.32] unit decrease |
| 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-14 |
| Odds Ratio | .17 [0.13-0.21] unit decrease |
[PMID 25675348] Evaluating the Association between Keratoconus and Reported Genetic Loci in a Han Chinese Population
