rs12144715
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs12144715(A;T) |
| Make rs12144715(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 84399547 |
| Gene | DNASE2B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12144715 |
| dbSNP (classic) | rs12144715 |
| ClinGen | rs12144715 |
| ebi | rs12144715 |
| HLI | rs12144715 |
| Exac | rs12144715 |
| Gnomad | rs12144715 |
| Varsome | rs12144715 |
| LitVar | rs12144715 |
| Map | rs12144715 |
| PheGenI | rs12144715 |
| Biobank | rs12144715 |
| 1000 genomes | rs12144715 |
| hgdp | rs12144715 |
| ensembl | rs12144715 |
| geneview | rs12144715 |
| scholar | rs12144715 |
| rs12144715 | |
| pharmgkb | rs12144715 |
| gwascentral | rs12144715 |
| openSNP | rs12144715 |
| 23andMe | rs12144715 |
| SNPshot | rs12144715 |
| SNPdbe | rs12144715 |
| MSV3d | rs12144715 |
| GWAS Ctlg | rs12144715 |
| GMAF | 0.07622 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22095909] |
| Trait | |
| Title | Serum ferritin levels are associated with a distinct phenotype of chronic hepatitis C poorly responding to pegylated interferon-alpha and ribavirin therapy. |
| Risk Allele | T |
| P-val | 0.000007 |
| Odds Ratio | 0.6360 None |
