rs7163757
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7163757(C;C) |
| Make rs7163757(C;T) |
| Make rs7163757(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 15 |
| Position | 62099409 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7163757 |
| dbSNP (classic) | rs7163757 |
| ClinGen | rs7163757 |
| ebi | rs7163757 |
| HLI | rs7163757 |
| Exac | rs7163757 |
| Gnomad | rs7163757 |
| Varsome | rs7163757 |
| LitVar | rs7163757 |
| Map | rs7163757 |
| PheGenI | rs7163757 |
| Biobank | rs7163757 |
| 1000 genomes | rs7163757 |
| hgdp | rs7163757 |
| ensembl | rs7163757 |
| geneview | rs7163757 |
| scholar | rs7163757 |
| rs7163757 | |
| pharmgkb | rs7163757 |
| gwascentral | rs7163757 |
| openSNP | rs7163757 |
| 23andMe | rs7163757 |
| SNPshot | rs7163757 |
| SNPdbe | rs7163757 |
| MSV3d | rs7163757 |
| GWAS Ctlg | rs7163757 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| 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 | C |
| P-val | 4E-6 |
| Odds Ratio | 1.06 [1.02-1.11] |
[PMID 27329800] Changes in the expression of the type 2 diabetes-associated gene VPS13C in the β cell are associated with glucose intolerance in humans and mice.
[PMID 29625024] A Common Type 2 Diabetes Risk Variant Potentiates Activity of an Evolutionarily Conserved Islet Stretch Enhancer and Increases C2CD4A and C2CD4B Expression.
