rs10898392
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10898392(G;G) |
| Make rs10898392(G;T) |
| Make rs10898392(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 85453707 |
| Gene | DLG2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10898392 |
| dbSNP (classic) | rs10898392 |
| ClinGen | rs10898392 |
| ebi | rs10898392 |
| HLI | rs10898392 |
| Exac | rs10898392 |
| Gnomad | rs10898392 |
| Varsome | rs10898392 |
| LitVar | rs10898392 |
| Map | rs10898392 |
| PheGenI | rs10898392 |
| Biobank | rs10898392 |
| 1000 genomes | rs10898392 |
| hgdp | rs10898392 |
| ensembl | rs10898392 |
| geneview | rs10898392 |
| scholar | rs10898392 |
| rs10898392 | |
| pharmgkb | rs10898392 |
| gwascentral | rs10898392 |
| openSNP | rs10898392 |
| 23andMe | rs10898392 |
| SNPshot | rs10898392 |
| SNPdbe | rs10898392 |
| MSV3d | rs10898392 |
| GWAS Ctlg | rs10898392 |
| GMAF | 0.4362 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19570815 ]
|
| Trait | Height |
| Title | A genome-wide association study of northwestern Europeans involves the CNP signaling pathway in the etiology of human height variation |
| Risk Allele | T |
| P-val | 0.000003 |
| Odds Ratio | NR NR |
