rs79047363
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs79047363(A;A) |
| Make rs79047363(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 73416262 |
| Gene | ALB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs79047363 |
| dbSNP (classic) | rs79047363 |
| ClinGen | rs79047363 |
| ebi | rs79047363 |
| HLI | rs79047363 |
| Exac | rs79047363 |
| Gnomad | rs79047363 |
| Varsome | rs79047363 |
| LitVar | rs79047363 |
| Map | rs79047363 |
| PheGenI | rs79047363 |
| Biobank | rs79047363 |
| 1000 genomes | rs79047363 |
| hgdp | rs79047363 |
| ensembl | rs79047363 |
| geneview | rs79047363 |
| scholar | rs79047363 |
| rs79047363 | |
| pharmgkb | rs79047363 |
| gwascentral | rs79047363 |
| openSNP | rs79047363 |
| 23andMe | rs79047363 |
| SNPshot | rs79047363 |
| SNPdbe | rs79047363 |
| MSV3d | rs79047363 |
| GWAS Ctlg | rs79047363 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs79047363(A;A) rs79047363(C;C) |
| Alt | rs79047363(A;A) rs79047363(C;C) |
| Reference | Rs79047363(G;G) |
| Significance | Other |
| Disease | ALBUMIN TOCHIGI ALBUMIN MALMO-5 |
| Variation | info |
| Gene | ALB |
| CLNDBN | ALBUMIN TOCHIGI ALBUMIN MALMO-5 |
| Reversed | 0 |
| HGVS | NC_000004.11:g.74281979G>A; NC_000004.11:g.74281979G>C |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000019847.1, RCV000019896.2, |
[PMID 2762316
] Point substitutions in Japanese alloalbumins.
[PMID 1518850] Alloalbuminemia in Sweden: structural study and phenotypic distribution of nine albumin variants.
