rs10226930
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common genotype |
| Make rs10226930(C;C) |
| Make rs10226930(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 156044601 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10226930 |
| dbSNP (classic) | rs10226930 |
| ClinGen | rs10226930 |
| ebi | rs10226930 |
| HLI | rs10226930 |
| Exac | rs10226930 |
| Gnomad | rs10226930 |
| Varsome | rs10226930 |
| LitVar | rs10226930 |
| Map | rs10226930 |
| PheGenI | rs10226930 |
| Biobank | rs10226930 |
| 1000 genomes | rs10226930 |
| hgdp | rs10226930 |
| ensembl | rs10226930 |
| geneview | rs10226930 |
| scholar | rs10226930 |
| rs10226930 | |
| pharmgkb | rs10226930 |
| gwascentral | rs10226930 |
| openSNP | rs10226930 |
| 23andMe | rs10226930 |
| SNPshot | rs10226930 |
| SNPdbe | rs10226930 |
| MSV3d | rs10226930 |
| GWAS Ctlg | rs10226930 |
| GMAF | 0.06107 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23322567 ]
|
| Trait | Corneal astigmatism |
| Title | Identification of a candidate gene for astigmatism. |
| Risk Allele | C |
| P-val | 8E-7 |
| Odds Ratio | 1.38 [NR] unit decrease |
