Rs1169310
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1169310 |
| PheGenI | rs1169310 |
| nextbio | rs1169310 |
| hapmap | rs1169310 |
| 1000 genomes | rs1169310 |
| hgdp | rs1169310 |
| ensembl | rs1169310 |
| gopubmed | rs1169310 |
| geneview | rs1169310 |
| scholar | rs1169310 |
| rs1169310 | |
| pharmgkb | rs1169310 |
| gwascentral | rs1169310 |
| openSNP | rs1169310 |
| 23andMe | rs1169310 |
| 23andMe all | rs1169310 |
| SNP Nexus | |
| SNPshot | rs1169310 |
| SNPdbe | rs1169310 |
| MSV3d | rs1169310 |
| Gene | HNF1A |
| Chromosome | 12 |
| Orientation | plus |
| GMAF | 0.3658 |
| Position | 121439433 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude |
| Make rs1169310(A;A) |
| Make rs1169310(A;G) |
| Make rs1169310(G;G) |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
| GWAS | |
|---|---|
| SNP | rs1169310 |
| PubMedID | [PMID 18439552] |
| Condition | C-reactive protein |
| Gene | HNF1A |
| Risk Allele | A |
| pValue | 2.00E-008 |
| OR | 0.13 |
| 95% CI | 0.08-0.17) mg/l decrease in log(CRP) leve |
[PMID 19474294] Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.
[PMID 21195701] Effect of obesity on the association between common variations in the HNF1A gene region and C-reactive protein level in Taiwanese.
| GET Evidence | |
|---|---|
| rs1169310 | |
| aa_change | |
| aa_change_short | |
| impact | pathogenic |
| qualified_impact | Insufficiently evaluated pathogenic |
| overall_frequency | 0.320312 |
| summary | |
