rs2844665
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs2844665(A;A) |
| Make rs2844665(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 31039078 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2844665 |
| dbSNP (classic) | rs2844665 |
| ClinGen | rs2844665 |
| ebi | rs2844665 |
| HLI | rs2844665 |
| Exac | rs2844665 |
| Gnomad | rs2844665 |
| Varsome | rs2844665 |
| LitVar | rs2844665 |
| Map | rs2844665 |
| PheGenI | rs2844665 |
| Biobank | rs2844665 |
| 1000 genomes | rs2844665 |
| hgdp | rs2844665 |
| ensembl | rs2844665 |
| geneview | rs2844665 |
| scholar | rs2844665 |
| rs2844665 | |
| pharmgkb | rs2844665 |
| gwascentral | rs2844665 |
| openSNP | rs2844665 |
| 23andMe | rs2844665 |
| SNPshot | rs2844665 |
| SNPdbe | rs2844665 |
| MSV3d | rs2844665 |
| GWAS Ctlg | rs2844665 |
| GMAF | 0.3843 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21801394 ]
|
| Trait | |
| Title | Genome-Wide Association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Europe. |
| Risk Allele | C |
| P-val | 3E-7 |
| Odds Ratio | 1.5400 [1.30-1.82] |
[PMID 26049586] A human leukocyte antigen locus haplotype confers risk for allopurinol-related adverse effects in Caucasian patients with gout
