rs11037909
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;T) | 1.1 | 1.27x type II diabetes risk |
| (T;T) | 1.2 | 1.47x type II diabetes risk |
| Make rs11037909(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 44234064 |
| Gene | EXT2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11037909 |
| dbSNP (classic) | rs11037909 |
| ClinGen | rs11037909 |
| ebi | rs11037909 |
| HLI | rs11037909 |
| Exac | rs11037909 |
| Gnomad | rs11037909 |
| Varsome | rs11037909 |
| LitVar | rs11037909 |
| Map | rs11037909 |
| PheGenI | rs11037909 |
| Biobank | rs11037909 |
| 1000 genomes | rs11037909 |
| hgdp | rs11037909 |
| ensembl | rs11037909 |
| geneview | rs11037909 |
| scholar | rs11037909 |
| rs11037909 | |
| pharmgkb | rs11037909 |
| gwascentral | rs11037909 |
| openSNP | rs11037909 |
| 23andMe | rs11037909 |
| SNPshot | rs11037909 |
| SNPdbe | rs11037909 |
| MSV3d | rs11037909 |
| GWAS Ctlg | rs11037909 |
| GMAF | 0.2966 |
| Max Magnitude | 1.2 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
rs11037909 increases susceptibility to Type II Diabetes 1.27 times for heterozygotes (CT) and 1.47 times for homozygotes (TT) [PMID 17293876]
[PMID 17786204
] Polymorphisms within novel risk loci for type 2 diabetes determine beta-cell function.
[PMID 18162508] Association of CDKAL1, IGF2BP2, CDKN2A/B, HHEX, SLC30A8, and KCNJ11 with susceptibility to type 2 diabetes in a Japanese population.
[PMID 18443202] Association analysis in african americans of European-derived type 2 diabetes single nucleotide polymorphisms from whole-genome association studies.
[PMID 18461161] Post genome-wide association studies of novel genes associated with type 2 diabetes show gene-gene interaction and high predictive value.
[PMID 18544707] Extension of type 2 diabetes genome-wide association scan results in the diabetes prevention program.
[PMID 18633108] Common variants in CDKAL1, CDKN2A/B, IGF2BP2, SLC30A8, and HHEX/IDE genes are associated with type 2 diabetes and impaired fasting glucose in a Chinese Han population.
[PMID 18689899] Exchangeable models of complex inherited diseases.
[PMID 20126254] Rare variants create synthetic genome-wide associations.
[PMID 22377712] Association between type 2 diabetes genetic susceptibility loci and visceral and subcutaneous fat area as determined by computed tomography.
[PMID 23052945] Association between variants of EXT2 and type 2 diabetes: a replication and meta-analysis
[PMID 25207843] Impact of variants of the EXT2 gene on Type 2 diabetes and its related traits in the Chinese han population
