rs2696297
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2696297(A;A) |
| Make rs2696297(A;G) |
| Make rs2696297(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 50167819 |
| Gene | LOC105371818, SGCA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2696297 |
| dbSNP (classic) | rs2696297 |
| ClinGen | rs2696297 |
| ebi | rs2696297 |
| HLI | rs2696297 |
| Exac | rs2696297 |
| Gnomad | rs2696297 |
| Varsome | rs2696297 |
| LitVar | rs2696297 |
| Map | rs2696297 |
| PheGenI | rs2696297 |
| Biobank | rs2696297 |
| 1000 genomes | rs2696297 |
| hgdp | rs2696297 |
| ensembl | rs2696297 |
| geneview | rs2696297 |
| scholar | rs2696297 |
| rs2696297 | |
| pharmgkb | rs2696297 |
| gwascentral | rs2696297 |
| openSNP | rs2696297 |
| 23andMe | rs2696297 |
| SNPshot | rs2696297 |
| SNPdbe | rs2696297 |
| MSV3d | rs2696297 |
| GWAS Ctlg | rs2696297 |
| GMAF | 0.1286 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
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| ||
[PMID 19714363] Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genes
