rs17044137
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17044137(A;A) |
| Make rs17044137(A;T) |
| Make rs17044137(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 111874141 |
| Gene | LOC105377369 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17044137 |
| dbSNP (classic) | rs17044137 |
| ClinGen | rs17044137 |
| ebi | rs17044137 |
| HLI | rs17044137 |
| Exac | rs17044137 |
| Gnomad | rs17044137 |
| Varsome | rs17044137 |
| LitVar | rs17044137 |
| Map | rs17044137 |
| PheGenI | rs17044137 |
| Biobank | rs17044137 |
| 1000 genomes | rs17044137 |
| hgdp | rs17044137 |
| ensembl | rs17044137 |
| geneview | rs17044137 |
| scholar | rs17044137 |
| rs17044137 | |
| pharmgkb | rs17044137 |
| gwascentral | rs17044137 |
| openSNP | rs17044137 |
| 23andMe | rs17044137 |
| SNPshot | rs17044137 |
| SNPdbe | rs17044137 |
| MSV3d | rs17044137 |
| GWAS Ctlg | rs17044137 |
| GMAF | 0.2392 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
| Rs17044137 | |
|---|---|
| PubMed | [PMID 17463246] |
| Affy Probeset | SNP_A-4271462 |
| Affy Orientation | same |
| On GW 5.0 | 1 |
| Alleles A/B | A/T |
| Ancestral | T |
| Population | NEU |
| Allele | A |
| Case Freq. | |
| Control Freq. | 0.23 |
| Odds Ratio Het | |
| Odds Ratio Hom | |
| Odds Ratio All | 1.13 |
| Disease | Type II Diabetes (T2D) |
rs17044137 increases susceptibility to Type II Diabetes 1.13 times for carriers of the A allele [PMID 17463246]
[PMID 18443202
] Association analysis in african americans of European-derived type 2 diabetes single nucleotide polymorphisms from whole-genome association studies.
[PMID 20126254] Rare variants create synthetic genome-wide associations.
