rs76285851
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs76285851(A;A) |
| Make rs76285851(A;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 73405117 |
| Gene | ALB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs76285851 |
| dbSNP (classic) | rs76285851 |
| ClinGen | rs76285851 |
| ebi | rs76285851 |
| HLI | rs76285851 |
| Exac | rs76285851 |
| Gnomad | rs76285851 |
| Varsome | rs76285851 |
| LitVar | rs76285851 |
| Map | rs76285851 |
| PheGenI | rs76285851 |
| Biobank | rs76285851 |
| 1000 genomes | rs76285851 |
| hgdp | rs76285851 |
| ensembl | rs76285851 |
| geneview | rs76285851 |
| scholar | rs76285851 |
| rs76285851 | |
| pharmgkb | rs76285851 |
| gwascentral | rs76285851 |
| openSNP | rs76285851 |
| 23andMe | rs76285851 |
| SNPshot | rs76285851 |
| SNPdbe | rs76285851 |
| MSV3d | rs76285851 |
| GWAS Ctlg | rs76285851 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs76285851(A;A) rs76285851(G;G) |
| Alt | rs76285851(A;A) rs76285851(G;G) |
| Reference | Rs76285851(C;C) |
| Significance | Other |
| Disease | ALBUMIN NAGASAKI 3 |
| Variation | info |
| Gene | ALB |
| CLNDBN | ALBUMIN NAGASAKI 3 |
| Reversed | 0 |
| HGVS | NC_000004.12:g.73405117C>R |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000019829.1, |
[PMID 3478700
] Structural changes and metal binding by proalbumins and other amino-terminal genetic variants of human serum albumin.
