rs11205277
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11205277(A;A) |
| Make rs11205277(A;G) |
| Make rs11205277(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 149920979 |
| Gene | LOC100507640 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11205277 |
| dbSNP (classic) | rs11205277 |
| ClinGen | rs11205277 |
| ebi | rs11205277 |
| HLI | rs11205277 |
| Exac | rs11205277 |
| Gnomad | rs11205277 |
| Varsome | rs11205277 |
| LitVar | rs11205277 |
| Map | rs11205277 |
| PheGenI | rs11205277 |
| Biobank | rs11205277 |
| 1000 genomes | rs11205277 |
| hgdp | rs11205277 |
| ensembl | rs11205277 |
| geneview | rs11205277 |
| scholar | rs11205277 |
| rs11205277 | |
| pharmgkb | rs11205277 |
| gwascentral | rs11205277 |
| openSNP | rs11205277 |
| 23andMe | rs11205277 |
| SNPshot | rs11205277 |
| SNPdbe | rs11205277 |
| MSV3d | rs11205277 |
| GWAS Ctlg | rs11205277 |
| GMAF | 0.2897 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 18391951] |
| Trait | Height |
| Title | Many sequence variants affecting diversity of adult human height |
| Risk Allele | G |
| P-val | 1E-10 |
| Odds Ratio | 5.10 [3.53-6.67] % SD taller |
[PMID 19039035
] Genome-wide association study identifies two novel loci containing FLNB and SBF2 genes underlying stature variation.
[PMID 20546612] The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature.
| GWAS snp | |
|---|---|
| PMID | [PMID 20881960]
|
| Trait | Height |
| Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
| Risk Allele | A |
| P-val | 5E-32 |
| Odds Ratio | .05 [NR] unit decrease |
