rs1726745
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1726745(A;A) |
| Make rs1726745(A;G) |
| Make rs1726745(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 74002397 |
| Gene | UCP3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1726745 |
| dbSNP (classic) | rs1726745 |
| ClinGen | rs1726745 |
| ebi | rs1726745 |
| HLI | rs1726745 |
| Exac | rs1726745 |
| Gnomad | rs1726745 |
| Varsome | rs1726745 |
| LitVar | rs1726745 |
| Map | rs1726745 |
| PheGenI | rs1726745 |
| Biobank | rs1726745 |
| 1000 genomes | rs1726745 |
| hgdp | rs1726745 |
| ensembl | rs1726745 |
| geneview | rs1726745 |
| scholar | rs1726745 |
| rs1726745 | |
| pharmgkb | rs1726745 |
| gwascentral | rs1726745 |
| openSNP | rs1726745 |
| 23andMe | rs1726745 |
| SNPshot | rs1726745 |
| SNPdbe | rs1726745 |
| MSV3d | rs1726745 |
| GWAS Ctlg | rs1726745 |
| GMAF | 0.4633 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19769793
] Variation in the UCP2 and UCP3 genes associates with abdominal obesity and serum lipids: The Finnish Diabetes Prevention Study
[PMID 24124336] Association between UCP3 gene polymorphisms and nonalcoholic fatty liver disease in Chinese children
