rs80106970
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs80106970(A;G) |
| Make rs80106970(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 73420257 |
| Gene | ALB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs80106970 |
| dbSNP (classic) | rs80106970 |
| ClinGen | rs80106970 |
| ebi | rs80106970 |
| HLI | rs80106970 |
| Exac | rs80106970 |
| Gnomad | rs80106970 |
| Varsome | rs80106970 |
| LitVar | rs80106970 |
| Map | rs80106970 |
| PheGenI | rs80106970 |
| Biobank | rs80106970 |
| 1000 genomes | rs80106970 |
| hgdp | rs80106970 |
| ensembl | rs80106970 |
| geneview | rs80106970 |
| scholar | rs80106970 |
| rs80106970 | |
| pharmgkb | rs80106970 |
| gwascentral | rs80106970 |
| openSNP | rs80106970 |
| 23andMe | rs80106970 |
| SNPshot | rs80106970 |
| SNPdbe | rs80106970 |
| MSV3d | rs80106970 |
| GWAS Ctlg | rs80106970 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs80106970(G;G) |
| Alt | rs80106970(G;G) |
| Reference | Rs80106970(A;A) |
| Significance | Non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | ALB |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000004.11:g.74285974A>G |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000019867.2, |
[PMID 3967761] Localization of the amino acid substitution site in a fast migrating variant of human serum albumin.
[PMID 15680241] Effect of genetic variation on the thermal stability of human serum albumin.
