rs2079795
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2079795(A;A) |
| Make rs2079795(A;G) |
| Make rs2079795(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 61419288 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2079795 |
| dbSNP (classic) | rs2079795 |
| ClinGen | rs2079795 |
| ebi | rs2079795 |
| HLI | rs2079795 |
| Exac | rs2079795 |
| Gnomad | rs2079795 |
| Varsome | rs2079795 |
| LitVar | rs2079795 |
| Map | rs2079795 |
| PheGenI | rs2079795 |
| Biobank | rs2079795 |
| 1000 genomes | rs2079795 |
| hgdp | rs2079795 |
| ensembl | rs2079795 |
| geneview | rs2079795 |
| scholar | rs2079795 |
| rs2079795 | |
| pharmgkb | rs2079795 |
| gwascentral | rs2079795 |
| openSNP | rs2079795 |
| 23andMe | rs2079795 |
| SNPshot | rs2079795 |
| SNPdbe | rs2079795 |
| MSV3d | rs2079795 |
| GWAS Ctlg | rs2079795 |
| GMAF | 0.3926 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19893584] |
| Trait | Height |
| Title | Identification of 15 loci influencing height in a Korean population |
| Risk Allele | T |
| P-val | 0.000003 |
| Odds Ratio | 0.40 [NR] cm increase |
[PMID 20027299
] Transferability and fine-mapping of genome-wide associated loci for adult height across human populations.
| 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 | 2E-24 |
| Odds Ratio | .04 [NR] unit increase |
| GWAS snp | |
|---|---|
| PMID | [PMID 23563607]
|
| Trait | Height |
| Title | Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. |
| Risk Allele | T |
| P-val | 1E-18 |
| Odds Ratio | 1.20 [NR] |
