rs79804069
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs79804069(A;C) |
| Make rs79804069(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 73412027 |
| Gene | ALB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs79804069 |
| dbSNP (classic) | rs79804069 |
| ClinGen | rs79804069 |
| ebi | rs79804069 |
| HLI | rs79804069 |
| Exac | rs79804069 |
| Gnomad | rs79804069 |
| Varsome | rs79804069 |
| LitVar | rs79804069 |
| Map | rs79804069 |
| PheGenI | rs79804069 |
| Biobank | rs79804069 |
| 1000 genomes | rs79804069 |
| hgdp | rs79804069 |
| ensembl | rs79804069 |
| geneview | rs79804069 |
| scholar | rs79804069 |
| rs79804069 | |
| pharmgkb | rs79804069 |
| gwascentral | rs79804069 |
| openSNP | rs79804069 |
| 23andMe | rs79804069 |
| SNPshot | rs79804069 |
| SNPdbe | rs79804069 |
| MSV3d | rs79804069 |
| GWAS Ctlg | rs79804069 |
| GMAF | 0.0004591 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs79804069(C;C) rs79804069(G;G) |
| Alt | rs79804069(C;C) rs79804069(G;G) |
| Reference | Rs79804069(A;A) |
| Significance | Other |
| Disease | ALBUMIN TRADATE 2 |
| Variation | info |
| Gene | ALB |
| CLNDBN | ALBUMIN TRADATE 2 |
| Reversed | 0 |
| HGVS | NC_000004.11:g.74277744A>C |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000019888.1, |
[PMID 8022807
] Genetic variants of human serum albumin in Italy: point mutants and a carboxyl-terminal variant.
