rs79744198
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs79744198(A;G) |
| Make rs79744198(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 73413454 |
| Gene | ALB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs79744198 |
| dbSNP (classic) | rs79744198 |
| ClinGen | rs79744198 |
| ebi | rs79744198 |
| HLI | rs79744198 |
| Exac | rs79744198 |
| Gnomad | rs79744198 |
| Varsome | rs79744198 |
| LitVar | rs79744198 |
| Map | rs79744198 |
| PheGenI | rs79744198 |
| Biobank | rs79744198 |
| 1000 genomes | rs79744198 |
| hgdp | rs79744198 |
| ensembl | rs79744198 |
| geneview | rs79744198 |
| scholar | rs79744198 |
| rs79744198 | |
| pharmgkb | rs79744198 |
| gwascentral | rs79744198 |
| openSNP | rs79744198 |
| 23andMe | rs79744198 |
| SNPshot | rs79744198 |
| SNPdbe | rs79744198 |
| MSV3d | rs79744198 |
| GWAS Ctlg | rs79744198 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs79744198(G;G) |
| Alt | rs79744198(G;G) |
| Reference | Rs79744198(A;A) |
| Significance | Non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | ALB |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000004.11:g.74279171A>G |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000019833.2, |
[PMID 2226433] Hormone binding to natural mutants of human serum albumin.
[PMID 2762316
] Point substitutions in Japanese alloalbumins.
[PMID 3594916] The molecular abnormality of albumin Niigata: 269 Asp----Gly.
