rs141733599
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs141733599(C;C) |
| Make rs141733599(C;T) |
| Make rs141733599(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 73404406 |
| Gene | ALB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs141733599 |
| dbSNP (classic) | rs141733599 |
| ClinGen | rs141733599 |
| ebi | rs141733599 |
| HLI | rs141733599 |
| Exac | rs141733599 |
| Gnomad | rs141733599 |
| Varsome | rs141733599 |
| LitVar | rs141733599 |
| Map | rs141733599 |
| PheGenI | rs141733599 |
| Biobank | rs141733599 |
| 1000 genomes | rs141733599 |
| hgdp | rs141733599 |
| ensembl | rs141733599 |
| geneview | rs141733599 |
| scholar | rs141733599 |
| rs141733599 | |
| pharmgkb | rs141733599 |
| gwascentral | rs141733599 |
| openSNP | rs141733599 |
| 23andMe | rs141733599 |
| SNPshot | rs141733599 |
| SNPdbe | rs141733599 |
| MSV3d | rs141733599 |
| GWAS Ctlg | rs141733599 |
| Merged from | Rs78611306 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs141733599(T;T) |
| Alt | rs141733599(T;T) |
| Reference | rs141733599(C;C) |
| Significance | Other |
| Disease | ALBUMIN LARINO |
| Variation | info |
| Gene | ALB |
| CLNDBN | ALBUMIN LARINO |
| Reversed | 0 |
| HGVS | NC_000004.11:g.74270123C>T |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000019887.2, |
[PMID 8022807
] Genetic variants of human serum albumin in Italy: point mutants and a carboxyl-terminal variant.
