rs3856806
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs3856806(C;T) |
| Make rs3856806(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 12434058 |
| Gene | PPARG |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3856806 |
| dbSNP (classic) | rs3856806 |
| ClinGen | rs3856806 |
| ebi | rs3856806 |
| HLI | rs3856806 |
| Exac | rs3856806 |
| Gnomad | rs3856806 |
| Varsome | rs3856806 |
| LitVar | rs3856806 |
| Map | rs3856806 |
| PheGenI | rs3856806 |
| Biobank | rs3856806 |
| 1000 genomes | rs3856806 |
| hgdp | rs3856806 |
| ensembl | rs3856806 |
| geneview | rs3856806 |
| scholar | rs3856806 |
| rs3856806 | |
| pharmgkb | rs3856806 |
| gwascentral | rs3856806 |
| openSNP | rs3856806 |
| 23andMe | rs3856806 |
| SNPshot | rs3856806 |
| SNPdbe | rs3856806 |
| MSV3d | rs3856806 |
| GWAS Ctlg | rs3856806 |
| GMAF | 0.1185 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20596649] PPARgamma polymorphisms and cancer risk: A meta-analysis involving 32,138 subjects
[PMID 21263402] Association of PPARG and LPIN1 gene polymorphisms with metabolic syndrome and type 2 diabetes
[PMID 21284483] Genetic Variants in Peroxisome Proliferator-Activated Receptor-? and Retinoid X Receptor-? Gene and Type 2 Diabetes Risk: A Case-Control Study of a Chinese Han Population
[PMID 22475777] Association Between PPAR-? and RXR-? Gene Polymorphism and Metabolic Syndrome Risk: A Case-Control Study of a Chinese Han Population
| ClinVar | |
|---|---|
| Risk | rs3856806(T;T) |
| Alt | rs3856806(T;T) |
| Reference | Rs3856806(C;C) |
| Significance | Probable-non-pathogenic |
| Disease | Glioma susceptibility 1 not specified Diabetes Mellitus Familial partial lipodystrophy Obesity |
| Variation | info |
| Gene | PPARG |
| CLNDBN | Glioma susceptibility 1 not specified Diabetes Mellitus, Noninsulin-Dependent, with Acanthosis Nigricans and Hypertension Familial partial lipodystrophy Obesity |
| Reversed | 0 |
| HGVS | NC_000003.11:g.12475557C>T |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000008615.3, RCV000118043.2, RCV000276900.1, RCV000331945.1, RCV000371595.1, |
[PMID 16713673] Variations in the peroxisome proliferator-activated receptor-gamma gene and melanoma risk.
[PMID 16783862] PPAR-gamma gene polymorphisms and psoriatic arthritis.
[PMID 17347532
] The Genetics of PPARG and the Skeleton.
[PMID 18160840] The association of Pro12Ala polymorphism of peroxisome proliferator-activated receptor-gamma gene with serum osteoprotegerin levels in healthy Korean women.
[PMID 18340007] Association of stearoyl-CoA desaturase 1 activity with familial combined hyperlipidemia.
[PMID 18375961] Polymorphism of genes related to insulin sensitivity and the risk of biliary tract cancer and biliary stone: a population-based case-control study in Shanghai, China.
[PMID 18401448] PPAR Genomics and Pharmacogenomics: Implications for Cardiovascular Disease.
[PMID 18426866] Association of FTO with obesity-related traits in the Cebu Longitudinal Health and Nutrition Survey (CLHNS) Cohort.
[PMID 18454203] Differential allelic expression in the human genome: a robust approach to identify genetic and epigenetic cis-acting mechanisms regulating gene expression.
[PMID 18603647] Functional genetic polymorphisms and female reproductive disorders: Part I: Polycystic ovary syndrome and ovarian response.
[PMID 18676870] Variants in inflammation genes and the risk of biliary tract cancers and stones: a population-based study in China.
[PMID 18707223] PPARG by dietary fat interaction influences bone mass in mice and humans.
[PMID 18805939] Functional genetic polymorphisms and female reproductive disorders: part II--endometriosis.
[PMID 18992148] Low-penetrance alleles predisposing to sporadic colorectal cancers: a French case-controlled genetic association study.
[PMID 19002430] Type 2 diabetes-associated genetic variants discovered in the recent genome-wide association studies are related to gestational diabetes mellitus in the Korean population.
[PMID 19041386] Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review.
[PMID 19208777] Genetic variation in the ADIPOR2 gene is associated with liver fat content and its surrogate markers in three independent cohorts.
[PMID 19223982] Genetic Variability of RXRB, PPARA, and PPARG in Wegener's Granulomatosis.
[PMID 20426853] Association and interaction of PPAR-complex gene variants with latent traits of left ventricular diastolic function.
[PMID 21140205] Joint effect of peroxisome proliferator-activated receptor gamma genetic polymorphisms and estrogen-related risk factors on breast cancer risk: results from a case-control study in Taiwan.
[PMID 21252350] Variants of the human PPARG locus and the susceptibility to chronic periodontitis.
[PMID 21756892] PPARG gene promoter polymorphism is associated with non-traumatic hip fracture risk in the elderly Slovenian population: a pilot study.
[PMID 22023374] Application of back propagation artificial neural network on genetic variants in adiponectin ADIPOQ, peroxisome proliferator-activated receptor-gamma, and retinoid X receptor-alpha genes and type 2 diabetes risk in a Chinese Han population.
[PMID 22410809] Association of PPAR-gamma gene polymorphisms with obesity and obesity-associated phenotypes in north indian population.
[PMID 22968028] [Association of both peroxisome proliferator-activated receptor, gene-gene interactions and the body mass index]
[PMID 23262340] Gene-gene interactions among PPARα/δ/γ polymorphisms for hypertriglyceridemia in Chinese Han population
[PMID 23741228] Lack of Genetic Associations of PPAR-γ and PGC-1α with Alzheimer's Disease and Parkinson's Disease with Dementia
[PMID 23545576] Association of peroxisome proliferator-activated receptor α/δ/γ with obesity, and gene-gene interaction, in the Chinese Han population
[PMID 23907334] Genetic Variants of Peroxisome Proliferator-Activated Receptor δ Are Associated with Gastric Cancer
[PMID 23937834] [Effects related to gene-gene interactions of peroxisome proliferator-activated receptor on essential hypertension]
[PMID 23363867] [Gene-gene interactions among the peroxisome proliferator-activated receptor polymorphisms for hypertriglyceridemia]
[PMID 22537818] Polymorphisms in adiposity-related genes are associated with age at menarche and menopause in breast cancer patients and healthy women.
[PMID 22987045] The meta-analysis of the association of PPARG P12A, C161T polymorphism and coronary heart disease.
[PMID 23533563] Novel risk factors for premature peripheral arterial occlusive disease in non-diabetic patients: a case-control study.
[PMID 25274455] The gene polymorphisms of UCP1 but not PPAR γ and TCF7L2 are associated with diabetic retinopathy in Chinese type 2 diabetes mellitus cases
[PMID 25832497] Association between Peroxisome Proliferator-activated Receptor Gamma Gene Polymorphisms and Atherosclerotic Diseases: A Meta-analysis of Case-control Studies
[PMID 26110145] Gene-Gene Interactions among Pparα/δ/γ Polymorphisms for Apolipoprotein (Apo) A-I/Apob Ratio in Chinese Han Population
[PMID 25422184] Lack of effects of peroxisome proliferator-activated receptor gamma genetic polymorphisms on breast cancer risk: a case-control study and pooled analysis
[PMID 26268872] [Association and interaction between 10 SNP of peroxisome proliferator-activated receptor and non-HDL-C]
[PMID 26550133] Peroxisome proliferator-activated receptor gamma (PPARG) polymorphisms and breast cancer susceptibility: a meta-analysis
[PMID 24599720] Effect of obesity on the association between common variations in the PPAR gene and C-reactive protein level in Chinese Han population
[PMID 26885119] Interaction between peroxisome proliferator- activated receptor gamma polymorphism and overweight on diabetic retinopathy in a Chinese case-control study.
[PMID 28123453] Interaction between peroxisome proliferator-activated receptor gamma polymorphism and obesity on type 2 diabetes in a Chinese Han population.
[PMID 31915541] PPARG Polymorphisms Are Associated with Unexplained Mild Vision Loss in Patients with Type 2 Diabetes Mellitus.
