rs1359790
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs1359790(C;T) |
| Make rs1359790(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 80143021 |
| Gene | LOC105370275 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1359790 |
| dbSNP (classic) | rs1359790 |
| ClinGen | rs1359790 |
| ebi | rs1359790 |
| HLI | rs1359790 |
| Exac | rs1359790 |
| Gnomad | rs1359790 |
| Varsome | rs1359790 |
| LitVar | rs1359790 |
| Map | rs1359790 |
| PheGenI | rs1359790 |
| Biobank | rs1359790 |
| 1000 genomes | rs1359790 |
| hgdp | rs1359790 |
| ensembl | rs1359790 |
| geneview | rs1359790 |
| scholar | rs1359790 |
| rs1359790 | |
| pharmgkb | rs1359790 |
| gwascentral | rs1359790 |
| openSNP | rs1359790 |
| 23andMe | rs1359790 |
| SNPshot | rs1359790 |
| SNPdbe | rs1359790 |
| MSV3d | rs1359790 |
| GWAS Ctlg | rs1359790 |
| GMAF | 0.2346 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20862305 ]
|
| Trait | |
| Title | Identification of new genetic risk variants for type 2 diabetes |
| Risk Allele | G |
| P-val | 6E-9 |
| Odds Ratio | 1.15 [1.10-1.20] |
[PMID 21909839] Genetic variants at CDC123/CAMK1D and SPRY2 are associated with susceptibility to type 2 diabetes in the Japanese population.
| GWAS snp | |
|---|---|
| PMID | [PMID 24509480]
|
| Trait | Type 2 diabetes |
| Title | Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. |
| Risk Allele | G |
| P-val | 6E-6 |
| Odds Ratio | 1.10 [1.05-1.14] |
