rs6469937
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6469937(A;A) |
| Make rs6469937(A;G) |
| Make rs6469937(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 120598198 |
| Gene | SNTB1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6469937 |
| dbSNP (classic) | rs6469937 |
| ClinGen | rs6469937 |
| ebi | rs6469937 |
| HLI | rs6469937 |
| Exac | rs6469937 |
| Gnomad | rs6469937 |
| Varsome | rs6469937 |
| LitVar | rs6469937 |
| Map | rs6469937 |
| PheGenI | rs6469937 |
| Biobank | rs6469937 |
| 1000 genomes | rs6469937 |
| hgdp | rs6469937 |
| ensembl | rs6469937 |
| geneview | rs6469937 |
| scholar | rs6469937 |
| rs6469937 | |
| pharmgkb | rs6469937 |
| gwascentral | rs6469937 |
| openSNP | rs6469937 |
| 23andMe | rs6469937 |
| SNPshot | rs6469937 |
| SNPdbe | rs6469937 |
| MSV3d | rs6469937 |
| GWAS Ctlg | rs6469937 |
| GMAF | 0.3972 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23933737] |
| Trait | Myopia (severe) |
| Title | Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia. |
| Risk Allele | A |
| P-val | 2E-9 |
| Odds Ratio | 1.27 [NR] |
[PMID 28848321
] Association and interaction of myopia with SNP markers rs13382811 and rs6469937 at ZFHX1B and SNTB1 in Han Chinese and European populations.
