rs678962
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs678962(G;G) |
| Make rs678962(G;T) |
| Make rs678962(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 172220749 |
| Gene | DNM3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs678962 |
| dbSNP (classic) | rs678962 |
| ClinGen | rs678962 |
| ebi | rs678962 |
| HLI | rs678962 |
| Exac | rs678962 |
| Gnomad | rs678962 |
| Varsome | rs678962 |
| LitVar | rs678962 |
| Map | rs678962 |
| PheGenI | rs678962 |
| Biobank | rs678962 |
| 1000 genomes | rs678962 |
| hgdp | rs678962 |
| ensembl | rs678962 |
| geneview | rs678962 |
| scholar | rs678962 |
| rs678962 | |
| pharmgkb | rs678962 |
| gwascentral | rs678962 |
| openSNP | rs678962 |
| 23andMe | rs678962 |
| SNPshot | rs678962 |
| SNPdbe | rs678962 |
| MSV3d | rs678962 |
| GWAS Ctlg | rs678962 |
| GMAF | 0.2645 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 18391951] |
| Trait | Height |
| Title | Many sequence variants affecting diversity of adult human height |
| Risk Allele | G |
| P-val | 2.9999999999999997E-8 |
| Odds Ratio | 5.40 [3.44-7.36] % SD taller |
[PMID 19197348
] Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae.
[PMID 20546612] The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature.
