rs1419881
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1419881(C;C) |
| Make rs1419881(C;T) |
| Make rs1419881(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 31162816 |
| Gene | TCF19 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1419881 |
| dbSNP (classic) | rs1419881 |
| ClinGen | rs1419881 |
| ebi | rs1419881 |
| HLI | rs1419881 |
| Exac | rs1419881 |
| Gnomad | rs1419881 |
| Varsome | rs1419881 |
| LitVar | rs1419881 |
| Map | rs1419881 |
| PheGenI | rs1419881 |
| Biobank | rs1419881 |
| 1000 genomes | rs1419881 |
| hgdp | rs1419881 |
| ensembl | rs1419881 |
| geneview | rs1419881 |
| scholar | rs1419881 |
| rs1419881 | |
| pharmgkb | rs1419881 |
| gwascentral | rs1419881 |
| openSNP | rs1419881 |
| 23andMe | rs1419881 |
| SNPshot | rs1419881 |
| SNPdbe | rs1419881 |
| MSV3d | rs1419881 |
| GWAS Ctlg | rs1419881 |
| GMAF | 0.4766 |
| 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 | 1E-18 |
| Odds Ratio | 1.37 [1.23-1.52] |
[PMID 24465836
] Genetic association of human leukocyte antigens with chronicity or resolution of hepatitis B infection in thai population
[PMID 18254969] Sequence variation in the human transcription factor gene POU5F1.
[PMID 18309376] Several regions in the major histocompatibility complex confer risk for anti-CCP-antibody positive rheumatoid arthritis, independent of the DRB1 locus.
[PMID 25802187] Genetic variants in five novel loci including CFB and CD40 predispose to chronic hepatitis B
[PMID 27596359] Identification of Novel OCT4 Genetic Variant Associated with the Risk of Chronic Hepatitis B in a Korean Population.
[PMID 27718532] Identification of miRSNPs associated with the risk of multiple myeloma.
