rs6718438
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6718438(C;C) |
| Make rs6718438(C;T) |
| Make rs6718438(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 232290856 |
| Gene | DIS3L2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6718438 |
| dbSNP (classic) | rs6718438 |
| ClinGen | rs6718438 |
| ebi | rs6718438 |
| HLI | rs6718438 |
| Exac | rs6718438 |
| Gnomad | rs6718438 |
| Varsome | rs6718438 |
| LitVar | rs6718438 |
| Map | rs6718438 |
| PheGenI | rs6718438 |
| Biobank | rs6718438 |
| 1000 genomes | rs6718438 |
| hgdp | rs6718438 |
| ensembl | rs6718438 |
| geneview | rs6718438 |
| scholar | rs6718438 |
| rs6718438 | |
| pharmgkb | rs6718438 |
| gwascentral | rs6718438 |
| openSNP | rs6718438 |
| 23andMe | rs6718438 |
| SNPshot | rs6718438 |
| SNPdbe | rs6718438 |
| MSV3d | rs6718438 |
| GWAS Ctlg | rs6718438 |
| GMAF | 0.4022 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19570815
] A genome-wide association study of northwestern Europeans involves the CNP signaling pathway in the etiology of human height variation
