Rs10492681
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10492681 |
| PheGenI | rs10492681 |
| nextbio | rs10492681 |
| hapmap | rs10492681 |
| 1000 genomes | rs10492681 |
| hgdp | rs10492681 |
| ensembl | rs10492681 |
| gopubmed | rs10492681 |
| geneview | rs10492681 |
| scholar | rs10492681 |
| rs10492681 | |
| pharmgkb | rs10492681 |
| gwascentral | rs10492681 |
| openSNP | rs10492681 |
| 23andMe | rs10492681 |
| 23andMe all | rs10492681 |
| SNP Nexus | |
| SNPshot | rs10492681 |
| SNPdbe | rs10492681 |
| MSV3d | rs10492681 |
| Chromosome | 13 |
| Orientation | plus |
| GMAF | 0.3063 |
| Position | 40807483 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude |
| Make rs10492681(C;C) |
| Make rs10492681(C;G) |
| Make rs10492681(G;G) |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
| GWAS snp | |
|---|---|
| PMID | [PMID 17903293] |
| Trait | Select biomarker traits |
| Title | Genome-wide association with select biomarker traits in the Framingham Heart Study |
| Risk Allele | |
| P-val | 0.0000019999999999999999 |
| Odds Ratio | NR NR |
| GET Evidence | |
|---|---|
| rs10492681 | |
| aa_change | |
| aa_change_short | |
| impact | pathogenic |
| qualified_impact | Insufficiently evaluated pathogenic |
| overall_frequency | 0.234375 |
| summary | |
