Rs10515148
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10515148 |
| PheGenI | rs10515148 |
| nextbio | rs10515148 |
| hapmap | rs10515148 |
| 1000 genomes | rs10515148 |
| hgdp | rs10515148 |
| ensembl | rs10515148 |
| gopubmed | rs10515148 |
| geneview | rs10515148 |
| scholar | rs10515148 |
| rs10515148 | |
| pharmgkb | rs10515148 |
| gwascentral | rs10515148 |
| openSNP | rs10515148 |
| 23andMe | rs10515148 |
| 23andMe all | rs10515148 |
| SNP Nexus | |
| SNPshot | rs10515148 |
| SNPdbe | rs10515148 |
| MSV3d | rs10515148 |
| Chromosome | 5 |
| Orientation | plus |
| GMAF | 0.1864 |
| Position | 71716928 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude |
| Make rs10515148(C;C) |
| Make rs10515148(C;G) |
| Make rs10515148(G;G) |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
| GWAS snp | |
|---|---|
| PMID | [PMID 17903296] |
| Trait | Hip geometry |
| Title | Genome-wide association with bone mass and geometry in the Framingham Heart Study |
| Risk Allele | |
| P-val | 5.9999999999999997E-7 |
| Odds Ratio | NR NR |
| GET Evidence | |
|---|---|
| rs10515148 | |
| aa_change | |
| aa_change_short | |
| impact | pathogenic |
| qualified_impact | Insufficiently evaluated pathogenic |
| overall_frequency | 0.164062 |
| summary | |
