rs2407103
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2407103(A;A) |
| Make rs2407103(A;G) |
| Make rs2407103(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 37094396 |
| Gene | LOC642879 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2407103 |
| dbSNP (classic) | rs2407103 |
| ClinGen | rs2407103 |
| ebi | rs2407103 |
| HLI | rs2407103 |
| Exac | rs2407103 |
| Gnomad | rs2407103 |
| Varsome | rs2407103 |
| LitVar | rs2407103 |
| Map | rs2407103 |
| PheGenI | rs2407103 |
| Biobank | rs2407103 |
| 1000 genomes | rs2407103 |
| hgdp | rs2407103 |
| ensembl | rs2407103 |
| geneview | rs2407103 |
| scholar | rs2407103 |
| rs2407103 | |
| pharmgkb | rs2407103 |
| gwascentral | rs2407103 |
| openSNP | rs2407103 |
| 23andMe | rs2407103 |
| SNPshot | rs2407103 |
| SNPdbe | rs2407103 |
| MSV3d | rs2407103 |
| GWAS Ctlg | rs2407103 |
| GMAF | 0.1327 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21901158 ]
|
| Trait | |
| Title | Genome-wide detection of allele specific copy number variation associated with insulin resistance in African Americans from the HyperGEN study. |
| Risk Allele | C |
| P-val | 0.000002 |
| Odds Ratio | 15.0000 [9.00 - 23.00] % increase |
