rs75523493
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs75523493(A;A) |
| Make rs75523493(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 73418232 |
| Gene | ALB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs75523493 |
| dbSNP (classic) | rs75523493 |
| ClinGen | rs75523493 |
| ebi | rs75523493 |
| HLI | rs75523493 |
| Exac | rs75523493 |
| Gnomad | rs75523493 |
| Varsome | rs75523493 |
| LitVar | rs75523493 |
| Map | rs75523493 |
| PheGenI | rs75523493 |
| Biobank | rs75523493 |
| 1000 genomes | rs75523493 |
| hgdp | rs75523493 |
| ensembl | rs75523493 |
| geneview | rs75523493 |
| scholar | rs75523493 |
| rs75523493 | |
| pharmgkb | rs75523493 |
| gwascentral | rs75523493 |
| openSNP | rs75523493 |
| 23andMe | rs75523493 |
| SNPshot | rs75523493 |
| SNPdbe | rs75523493 |
| MSV3d | rs75523493 |
| GWAS Ctlg | rs75523493 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs75523493(A;A) |
| Alt | rs75523493(A;A) |
| Reference | Rs75523493(G;G) |
| Significance | Other |
| Disease | ALBUMIN VANCOUVER |
| Variation | info |
| Gene | ALB |
| CLNDBN | ALBUMIN VANCOUVER |
| Reversed | 0 |
| HGVS | NC_000004.11:g.74283949G>A |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000019851.1, |
[PMID 2317208
] Genetic characterization of an alloalbumin, albumin Kashmir, using gene amplification and allele-specific oligonucleotides.
[PMID 2404284] Point substitutions in albumin genetic variants from Asia.
