rs3997872
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs3997872(A;A) |
| Make rs3997872(A;T) |
| Make rs3997872(T;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 6 |
| Position | 32612840 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3997872 |
| dbSNP (classic) | rs3997872 |
| ClinGen | rs3997872 |
| ebi | rs3997872 |
| HLI | rs3997872 |
| Exac | rs3997872 |
| Gnomad | rs3997872 |
| Varsome | rs3997872 |
| LitVar | rs3997872 |
| Map | rs3997872 |
| PheGenI | rs3997872 |
| Biobank | rs3997872 |
| 1000 genomes | rs3997872 |
| hgdp | rs3997872 |
| ensembl | rs3997872 |
| geneview | rs3997872 |
| scholar | rs3997872 |
| rs3997872 | |
| pharmgkb | rs3997872 |
| gwascentral | rs3997872 |
| openSNP | rs3997872 |
| 23andMe | rs3997872 |
| SNPshot | rs3997872 |
| SNPdbe | rs3997872 |
| MSV3d | rs3997872 |
| GWAS Ctlg | rs3997872 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 26538132
] Genetic variations in STAT4,C2,HLA-DRB1 and HLA-DQ associated with risk of hepatitis B virus-related liver cirrhosis
