rs3815087
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3815087(C;C) |
| Make rs3815087(C;T) |
| Make rs3815087(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 31125810 |
| Gene | PSORS1C1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3815087 |
| dbSNP (classic) | rs3815087 |
| ClinGen | rs3815087 |
| ebi | rs3815087 |
| HLI | rs3815087 |
| Exac | rs3815087 |
| Gnomad | rs3815087 |
| Varsome | rs3815087 |
| LitVar | rs3815087 |
| Map | rs3815087 |
| PheGenI | rs3815087 |
| Biobank | rs3815087 |
| 1000 genomes | rs3815087 |
| hgdp | rs3815087 |
| ensembl | rs3815087 |
| geneview | rs3815087 |
| scholar | rs3815087 |
| rs3815087 | |
| pharmgkb | rs3815087 |
| gwascentral | rs3815087 |
| openSNP | rs3815087 |
| 23andMe | rs3815087 |
| SNPshot | rs3815087 |
| SNPdbe | rs3815087 |
| MSV3d | rs3815087 |
| GWAS Ctlg | rs3815087 |
| GMAF | 0.2769 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20041166 ]
|
| Trait | HIV-1 control |
| Title | Common Genetic Variation and the Control of HIV-1 in Human |
| Risk Allele | |
| P-val | 8E-8 |
| Odds Ratio | NR NR |
| GWAS snp | |
|---|---|
| PMID | [PMID 21801394]
|
| Trait | |
| Title | Genome-Wide Association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Europe. |
| Risk Allele | A |
| P-val | 3E-7 |
| Odds Ratio | 1.5300 [1.29-1.80] |
