rs1048466
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1048466(A;A) |
| Make rs1048466(A;G) |
| Make rs1048466(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 442384 |
| Gene | CCDC77 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1048466 |
| dbSNP (classic) | rs1048466 |
| ClinGen | rs1048466 |
| ebi | rs1048466 |
| HLI | rs1048466 |
| Exac | rs1048466 |
| Gnomad | rs1048466 |
| Varsome | rs1048466 |
| LitVar | rs1048466 |
| Map | rs1048466 |
| PheGenI | rs1048466 |
| Biobank | rs1048466 |
| 1000 genomes | rs1048466 |
| hgdp | rs1048466 |
| ensembl | rs1048466 |
| geneview | rs1048466 |
| scholar | rs1048466 |
| rs1048466 | |
| pharmgkb | rs1048466 |
| gwascentral | rs1048466 |
| openSNP | rs1048466 |
| 23andMe | rs1048466 |
| SNPshot | rs1048466 |
| SNPdbe | rs1048466 |
| MSV3d | rs1048466 |
| GWAS Ctlg | rs1048466 |
| GMAF | 0.242 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23563609 ]
|
| Trait | Obesity (early onset extreme) |
| Title | Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity. |
| Risk Allele | G |
| P-val | 8E-8 |
| Odds Ratio | 1.22 [1.14-1.32] |
