rs78611306
From SNPedia
| Merged into | rs141733599 |
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs78611306(C;C) |
| Make rs78611306(C;T) |
| Make rs78611306(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 73404406 |
| Gene | ALB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs78611306 |
| dbSNP (classic) | rs78611306 |
| ClinGen | rs78611306 |
| ebi | rs78611306 |
| HLI | rs78611306 |
| Exac | rs78611306 |
| Gnomad | rs78611306 |
| Varsome | rs78611306 |
| LitVar | rs78611306 |
| Map | rs78611306 |
| PheGenI | rs78611306 |
| Biobank | rs78611306 |
| 1000 genomes | rs78611306 |
| hgdp | rs78611306 |
| ensembl | rs78611306 |
| geneview | rs78611306 |
| scholar | rs78611306 |
| rs78611306 | |
| pharmgkb | rs78611306 |
| gwascentral | rs78611306 |
| openSNP | rs78611306 |
| 23andMe | rs78611306 |
| SNPshot | rs78611306 |
| SNPdbe | rs78611306 |
| MSV3d | rs78611306 |
| GWAS Ctlg | rs78611306 |
| Status | Merged into rs141733599 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs78611306(C;C) rs78611306(T;T) |
| Alt | rs78611306(C;C) rs78611306(T;T) |
| Reference | Rs78611306(G;G) |
| Significance | Untested |
| Disease | |
| Variation | info |
| Gene | ALB |
| CLNDBN | |
| Reversed | 0 |
| HGVS | NC_000004.11:g.74270832G>C |
| CLNSRC | |
| CLNACC | |
[PMID 8022807
] Genetic variants of human serum albumin in Italy: point mutants and a carboxyl-terminal variant.
