rs757210
| Orientation | minus |
| Stabilized | minus |
| Make rs757210(A;A) |
| Make rs757210(A;G) |
| Make rs757210(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 37736525 |
| Gene | HNF1B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs757210 |
| dbSNP (classic) | rs757210 |
| ClinGen | rs757210 |
| ebi | rs757210 |
| HLI | rs757210 |
| Exac | rs757210 |
| Gnomad | rs757210 |
| Varsome | rs757210 |
| LitVar | rs757210 |
| Map | rs757210 |
| PheGenI | rs757210 |
| Biobank | rs757210 |
| 1000 genomes | rs757210 |
| hgdp | rs757210 |
| ensembl | rs757210 |
| geneview | rs757210 |
| scholar | rs757210 |
| rs757210 | |
| pharmgkb | rs757210 |
| gwascentral | rs757210 |
| openSNP | rs757210 |
| 23andMe | rs757210 |
| SNPshot | rs757210 |
| SNPdbe | rs757210 |
| MSV3d | rs757210 |
| GWAS Ctlg | rs757210 |
| GMAF | 0.3788 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19502414
] Association of 18 confirmed susceptibility loci for type 2 diabetes with indices of insulin release, proinsulin conversion, and insulin sensitivity in 5,327 nondiabetic Finnish men
[PMID 21421807] In a study conducted on 6,580 Nondiabetic Finnish Men, rs757210 in HNF1B gene showed nominal or significant associations with several lipoprotein traits.
[PMID 22052079] Association analysis of 31 common polymorphisms with type 2 diabetes and its related traits in Indian sib pairs
[PMID 17327436] Evaluation of common variants in the six known maturity-onset diabetes of the young (MODY) genes for association with type 2 diabetes.
[PMID 18426861] Association analysis of type 2 diabetes Loci in type 1 diabetes.
[PMID 18591388] Assessing the combined impact of 18 common genetic variants of modest effect sizes on type 2 diabetes risk.
[PMID 18701471] Chromosome 17q12 variants contribute to risk of early-onset prostate cancer.
[PMID 18782870] Clinical review: the genetics of type 2 diabetes: a realistic appraisal in 2008.
[PMID 19056611] Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data.
[PMID 19168595] Common variants of hepatocyte nuclear factor 1beta are associated with type 2 diabetes in a Chinese population.
[PMID 19207020] Meta-analysis in genome-wide association studies.
[PMID 19323962] Genome-wide association studies in type 2 diabetes.
[PMID 19341491] Genome-based prediction of common diseases: methodological considerations for future research.
[PMID 19460916] Genetic architecture of type 2 diabetes: recent progress and clinical implications.
[PMID 19602701] Underlying genetic models of inheritance in established type 2 diabetes associations.
[PMID 20017978] Influence of control selection in genome-wide association studies: the example of diabetes in the Framingham Heart Study.
[PMID 20018041] The effect of multiple genetic variants in predicting the risk of type 2 diabetes.
[PMID 20043853] Prioritizing genes for follow-up from genome wide association studies using information on gene expression in tissues relevant for type 2 diabetes mellitus.
[PMID 20712903] Obesity and diabetes genes are associated with being born small for gestational age: results from the Auckland Birthweight Collaborative study.
[PMID 21278902] Genetic risk profiling for prediction of type 2 diabetes.
[PMID 22022982] Alternative methods to a TaqMan assay to detect a tri-allelic single nucleotide polymorphism rs757210 in the HNF1beta gene.
[PMID 23193118] Association of Type 2 Diabetes Susceptibility Variants With Advanced Prostate Cancer Risk in the Breast and Prostate Cancer Cohort Consortium
| GWAS snp | |
|---|---|
| PMID | [PMID 23535730]
|
| Trait | Ovarian cancer |
| Title | GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer. |
| Risk Allele | G |
| P-val | 8E-10 |
| Odds Ratio | 1.12 [1.08-1.17] |
[PMID 31860786] A diabetes-associated genetic variant is associated with diastolic dysfunction and cardiovascular disease.
