rs2736654
From SNPedia
| Merged into | rs4746 |
| Orientation | minus |
| Stabilized | minus |
| Make rs2736654(A;A) |
| Make rs2736654(A;C) |
| Make rs2736654(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 38682852 |
| Gene | GLO1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2736654 |
| dbSNP (classic) | rs2736654 |
| ClinGen | rs2736654 |
| ebi | rs2736654 |
| HLI | rs2736654 |
| Exac | rs2736654 |
| Gnomad | rs2736654 |
| Varsome | rs2736654 |
| LitVar | rs2736654 |
| Map | rs2736654 |
| PheGenI | rs2736654 |
| Biobank | rs2736654 |
| 1000 genomes | rs2736654 |
| hgdp | rs2736654 |
| ensembl | rs2736654 |
| geneview | rs2736654 |
| scholar | rs2736654 |
| rs2736654 | |
| pharmgkb | rs2736654 |
| gwascentral | rs2736654 |
| openSNP | rs2736654 |
| 23andMe | rs2736654 |
| SNPshot | rs2736654 |
| SNPdbe | rs2736654 |
| MSV3d | rs2736654 |
| GWAS Ctlg | rs2736654 |
| Status | Merged into rs4746 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 19412133] Polymorphisms in glyoxalase 1 gene are not associated with vascular complications: the Hoorn and CoDAM studies
[PMID 21491613
] Glyoxalase I polymorphism rs2736654 causing the Ala111Glu substitution modulates enzyme activity-implications for autism
