rs6744284
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6744284(C;C) |
| Make rs6744284(C;T) |
| Make rs6744284(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 233716651 |
| Gene | UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6744284 |
| dbSNP (classic) | rs6744284 |
| ClinGen | rs6744284 |
| ebi | rs6744284 |
| HLI | rs6744284 |
| Exac | rs6744284 |
| Gnomad | rs6744284 |
| Varsome | rs6744284 |
| LitVar | rs6744284 |
| Map | rs6744284 |
| PheGenI | rs6744284 |
| Biobank | rs6744284 |
| 1000 genomes | rs6744284 |
| hgdp | rs6744284 |
| ensembl | rs6744284 |
| geneview | rs6744284 |
| scholar | rs6744284 |
| rs6744284 | |
| pharmgkb | rs6744284 |
| gwascentral | rs6744284 |
| openSNP | rs6744284 |
| 23andMe | rs6744284 |
| SNPshot | rs6744284 |
| SNPdbe | rs6744284 |
| MSV3d | rs6744284 |
| GWAS Ctlg | rs6744284 |
| GMAF | 0.3297 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 22511988
] A Genome-Wide Association Study Identifies UGT1A1 as a Regulator of Serum Cell-Free DNA in Young Adults: The Cardiovascular Risk in Young Finns Study
[PMID 21291537] Evidence for somatic gene conversion and deletion in bipolar disorder, Crohn's disease, coronary artery disease, hypertension, rheumatoid arthritis, type-1 diabetes, and type-2 diabetes.
