rs6449353
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6449353(C;C) |
| Make rs6449353(C;T) |
| Make rs6449353(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 18031865 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6449353 |
| dbSNP (classic) | rs6449353 |
| ClinGen | rs6449353 |
| ebi | rs6449353 |
| HLI | rs6449353 |
| Exac | rs6449353 |
| Gnomad | rs6449353 |
| Varsome | rs6449353 |
| LitVar | rs6449353 |
| Map | rs6449353 |
| PheGenI | rs6449353 |
| Biobank | rs6449353 |
| 1000 genomes | rs6449353 |
| hgdp | rs6449353 |
| ensembl | rs6449353 |
| geneview | rs6449353 |
| scholar | rs6449353 |
| rs6449353 | |
| pharmgkb | rs6449353 |
| gwascentral | rs6449353 |
| openSNP | rs6449353 |
| 23andMe | rs6449353 |
| SNPshot | rs6449353 |
| SNPdbe | rs6449353 |
| MSV3d | rs6449353 |
| GWAS Ctlg | rs6449353 |
| GMAF | 0.2218 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20881960 ]
|
| Trait | Height |
| Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
| Risk Allele | T |
| P-val | 7E-46 |
| Odds Ratio | .08 [NR] unit increase |
