rs1436955
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1436955(A;A) |
| Make rs1436955(A;G) |
| Make rs1436955(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 62112183 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1436955 |
| dbSNP (classic) | rs1436955 |
| ClinGen | rs1436955 |
| ebi | rs1436955 |
| HLI | rs1436955 |
| Exac | rs1436955 |
| Gnomad | rs1436955 |
| Varsome | rs1436955 |
| LitVar | rs1436955 |
| Map | rs1436955 |
| PheGenI | rs1436955 |
| Biobank | rs1436955 |
| 1000 genomes | rs1436955 |
| hgdp | rs1436955 |
| ensembl | rs1436955 |
| geneview | rs1436955 |
| scholar | rs1436955 |
| rs1436955 | |
| pharmgkb | rs1436955 |
| gwascentral | rs1436955 |
| openSNP | rs1436955 |
| 23andMe | rs1436955 |
| SNPshot | rs1436955 |
| SNPdbe | rs1436955 |
| MSV3d | rs1436955 |
| GWAS Ctlg | rs1436955 |
| GMAF | 0.3035 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20862305 ]
|
| Trait | |
| Title | Identification of new genetic risk variants for type 2 diabetes |
| Risk Allele | C |
| P-val | 7E-7 |
| Odds Ratio | 1.13 [1.08-1.19] |
[PMID 21909839] Genetic variants at CDC123/CAMK1D and SPRY2 are associated with susceptibility to type 2 diabetes in the Japanese population.
