rs16864968
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs16864968(A;G) |
| Make rs16864968(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 223594965 |
| Gene | SCG2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16864968 |
| dbSNP (classic) | rs16864968 |
| ClinGen | rs16864968 |
| ebi | rs16864968 |
| HLI | rs16864968 |
| Exac | rs16864968 |
| Gnomad | rs16864968 |
| Varsome | rs16864968 |
| LitVar | rs16864968 |
| Map | rs16864968 |
| PheGenI | rs16864968 |
| Biobank | rs16864968 |
| 1000 genomes | rs16864968 |
| hgdp | rs16864968 |
| ensembl | rs16864968 |
| geneview | rs16864968 |
| scholar | rs16864968 |
| rs16864968 | |
| pharmgkb | rs16864968 |
| gwascentral | rs16864968 |
| openSNP | rs16864968 |
| 23andMe | rs16864968 |
| SNPshot | rs16864968 |
| SNPdbe | rs16864968 |
| MSV3d | rs16864968 |
| GWAS Ctlg | rs16864968 |
| GMAF | 0.1428 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 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 | G |
| P-val | 0.000003 |
| Odds Ratio | 0.8260 None |
