rs652888
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs652888(C;C) |
| Make rs652888(C;T) |
| Make rs652888(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 31883457 |
| Gene | EHMT2, LOC107986588 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs652888 |
| dbSNP (classic) | rs652888 |
| ClinGen | rs652888 |
| ebi | rs652888 |
| HLI | rs652888 |
| Exac | rs652888 |
| Gnomad | rs652888 |
| Varsome | rs652888 |
| LitVar | rs652888 |
| Map | rs652888 |
| PheGenI | rs652888 |
| Biobank | rs652888 |
| 1000 genomes | rs652888 |
| hgdp | rs652888 |
| ensembl | rs652888 |
| geneview | rs652888 |
| scholar | rs652888 |
| rs652888 | |
| pharmgkb | rs652888 |
| gwascentral | rs652888 |
| openSNP | rs652888 |
| 23andMe | rs652888 |
| SNPshot | rs652888 |
| SNPdbe | rs652888 |
| MSV3d | rs652888 |
| GWAS Ctlg | rs652888 |
| GMAF | 0.1983 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23760081] |
| Trait | Chronic hepatitis B infection |
| Title | A genome-wide association study identified new variants associated with the risk of chronic hepatitis B. |
| Risk Allele | |
| P-val | 7E-13 |
| Odds Ratio | 1.38 [1.22-1.57] |
[PMID 24465836
] Genetic association of human leukocyte antigens with chronicity or resolution of hepatitis B infection in thai population
[PMID 18204098] Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX.
[PMID 25802187] Genetic variants in five novel loci including CFB and CD40 predispose to chronic hepatitis B
[PMID 27157822] Genetic variants associated with antithyroid drug-induced agranulocytosis: a genome-wide association study in a European population.
[PMID 29238036] Identification of additional EHMT2 variant associated with the risk of chronic hepatitis B by GWAS follow-up study.
