rs10838687
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10838687(G;G) |
| Make rs10838687(G;T) |
| Make rs10838687(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 47291341 |
| Gene | MADD |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10838687 |
| dbSNP (classic) | rs10838687 |
| ClinGen | rs10838687 |
| ebi | rs10838687 |
| HLI | rs10838687 |
| Exac | rs10838687 |
| Gnomad | rs10838687 |
| Varsome | rs10838687 |
| LitVar | rs10838687 |
| Map | rs10838687 |
| PheGenI | rs10838687 |
| Biobank | rs10838687 |
| 1000 genomes | rs10838687 |
| hgdp | rs10838687 |
| ensembl | rs10838687 |
| geneview | rs10838687 |
| scholar | rs10838687 |
| rs10838687 | |
| pharmgkb | rs10838687 |
| gwascentral | rs10838687 |
| openSNP | rs10838687 |
| 23andMe | rs10838687 |
| SNPshot | rs10838687 |
| SNPdbe | rs10838687 |
| MSV3d | rs10838687 |
| GWAS Ctlg | rs10838687 |
| GMAF | 0.382 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21873549 ]
|
| Trait | |
| Title | Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes. |
| Risk Allele | T |
| P-val | 7E-12 |
| Odds Ratio | None None |
[PMID 24951664] Association of Levels of Fasting Glucose and Insulin With Rare Variants at the Chromosome 11p11.2-MADD Locus: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study
