rs6576507
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs6576507(C;C) |
| Make rs6576507(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 26043247 |
| Gene | LOC100128714 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6576507 |
| dbSNP (classic) | rs6576507 |
| ClinGen | rs6576507 |
| ebi | rs6576507 |
| HLI | rs6576507 |
| Exac | rs6576507 |
| Gnomad | rs6576507 |
| Varsome | rs6576507 |
| LitVar | rs6576507 |
| Map | rs6576507 |
| PheGenI | rs6576507 |
| Biobank | rs6576507 |
| 1000 genomes | rs6576507 |
| hgdp | rs6576507 |
| ensembl | rs6576507 |
| geneview | rs6576507 |
| scholar | rs6576507 |
| rs6576507 | |
| pharmgkb | rs6576507 |
| gwascentral | rs6576507 |
| openSNP | rs6576507 |
| 23andMe | rs6576507 |
| SNPshot | rs6576507 |
| SNPdbe | rs6576507 |
| MSV3d | rs6576507 |
| GWAS Ctlg | rs6576507 |
| GMAF | 0.03994 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 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 | A |
| P-val | 4E-7 |
| Odds Ratio | 14.0000 [8.00-20.00] % increase |
