rs4548577
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4548577(C;C) |
| Make rs4548577(C;T) |
| Make rs4548577(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 46976961 |
| Gene | C11orf49 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4548577 |
| dbSNP (classic) | rs4548577 |
| ClinGen | rs4548577 |
| ebi | rs4548577 |
| HLI | rs4548577 |
| Exac | rs4548577 |
| Gnomad | rs4548577 |
| Varsome | rs4548577 |
| LitVar | rs4548577 |
| Map | rs4548577 |
| PheGenI | rs4548577 |
| Biobank | rs4548577 |
| 1000 genomes | rs4548577 |
| hgdp | rs4548577 |
| ensembl | rs4548577 |
| geneview | rs4548577 |
| scholar | rs4548577 |
| rs4548577 | |
| pharmgkb | rs4548577 |
| gwascentral | rs4548577 |
| openSNP | rs4548577 |
| 23andMe | rs4548577 |
| SNPshot | rs4548577 |
| SNPdbe | rs4548577 |
| MSV3d | rs4548577 |
| GWAS Ctlg | rs4548577 |
| GMAF | 0.314 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| Rs4548577 | |
|---|---|
| PubMed | [PMID 18445777] |
| Affy Probeset | SNP_A-2158992 |
| Affy Orientation | same |
| On GW 5.0 | |
| Alleles A/B | C/T |
| Ancestral | C |
| Population | Caucasian |
| Allele | C |
| Case Freq. | |
| Control Freq. | |
| Odds Ratio Het | |
| Odds Ratio Hom | |
| Odds Ratio All | 1.08 |
| Disease | Osteoporotic fractures (OP-F) |
rs4548577 is in linkage disequilibrium with a polymorphism that increases susceptibility to Osteoporotic fractures 1.08 times for carriers of the C allele [PMID 18445777]
