rs3101336
| Orientation | minus |
| Stabilized | minus |
| Make rs3101336(A;A) |
| Make rs3101336(A;G) |
| Make rs3101336(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 72285502 |
| Gene | LOC105378797 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3101336 |
| dbSNP (classic) | rs3101336 |
| ClinGen | rs3101336 |
| ebi | rs3101336 |
| HLI | rs3101336 |
| Exac | rs3101336 |
| Gnomad | rs3101336 |
| Varsome | rs3101336 |
| LitVar | rs3101336 |
| Map | rs3101336 |
| PheGenI | rs3101336 |
| Biobank | rs3101336 |
| 1000 genomes | rs3101336 |
| hgdp | rs3101336 |
| ensembl | rs3101336 |
| geneview | rs3101336 |
| scholar | rs3101336 |
| rs3101336 | |
| pharmgkb | rs3101336 |
| gwascentral | rs3101336 |
| openSNP | rs3101336 |
| 23andMe | rs3101336 |
| SNPshot | rs3101336 |
| SNPdbe | rs3101336 |
| MSV3d | rs3101336 |
| GWAS Ctlg | rs3101336 |
| GMAF | 0.3012 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20061430] Obesity Susceptibility Genetic Variants Identified from Recent Genome-Wide Association Studies: Implications in a Chinese Population
[PMID 22384102
] A Latent Variable Partial Least Squares Path Modeling Approach to Regional Association and Polygenic Effect with Applications to a Human Obesity Study
[PMID 19478790
] The role of obesity-associated loci identified in genome-wide association studies in the determination of pediatric BMI.
[PMID 20824172
] Physical activity attenuates the genetic predisposition to obesity in 20,000 men and women from EPIC-Norfolk prospective population study.
[PMID 21750520
] Implication of European-derived adiposity loci in African Americans.
| GWAS snp | |
|---|---|
| PMID | [PMID 23563607 |
| Trait | Obesity |
| Title | Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. |
| Risk Allele | C |
| P-val | 1E-13 |
| Odds Ratio | 1.12 [NR] |
| 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 | C |
| P-val | 2E-8 |
| Odds Ratio | 1.21 [1.13-1.29] |
