Rs11648796
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11648796 |
| PheGenI | rs11648796 |
| nextbio | rs11648796 |
| hapmap | rs11648796 |
| 1000 genomes | rs11648796 |
| hgdp | rs11648796 |
| ensembl | rs11648796 |
| gopubmed | rs11648796 |
| geneview | rs11648796 |
| scholar | rs11648796 |
| rs11648796 | |
| pharmgkb | rs11648796 |
| gwascentral | rs11648796 |
| openSNP | rs11648796 |
| 23andMe | rs11648796 |
| 23andMe all | rs11648796 |
| SNP Nexus | |
| SNPshot | rs11648796 |
| SNPdbe | rs11648796 |
| MSV3d | rs11648796 |
| Gene | NARFL |
| Chromosome | 16 |
| Orientation | plus |
| GMAF | 0.4844 |
| Position | 792190 |
| Reference | GRCh37.p2 37.2/134 |
| Max Magnitude |
| Make rs11648796(A;A) |
| Make rs11648796(A;G) |
| Make rs11648796(G;G) |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
| GWAS snp | |
|---|---|
| PMID | [PMID 20881960] |
| Trait | |
| Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
| Risk Allele | A |
| P-val | 1E-13 |
| Odds Ratio | 0.0300 [NR] meters decrease |
