rs76454301
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs76454301(A;A) |
| Make rs76454301(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 73411996 |
| Gene | ALB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs76454301 |
| dbSNP (classic) | rs76454301 |
| ClinGen | rs76454301 |
| ebi | rs76454301 |
| HLI | rs76454301 |
| Exac | rs76454301 |
| Gnomad | rs76454301 |
| Varsome | rs76454301 |
| LitVar | rs76454301 |
| Map | rs76454301 |
| PheGenI | rs76454301 |
| Biobank | rs76454301 |
| 1000 genomes | rs76454301 |
| hgdp | rs76454301 |
| ensembl | rs76454301 |
| geneview | rs76454301 |
| scholar | rs76454301 |
| rs76454301 | |
| pharmgkb | rs76454301 |
| gwascentral | rs76454301 |
| openSNP | rs76454301 |
| 23andMe | rs76454301 |
| SNPshot | rs76454301 |
| SNPdbe | rs76454301 |
| MSV3d | rs76454301 |
| GWAS Ctlg | rs76454301 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs76454301(A;A) rs76454301(C;C) |
| Alt | rs76454301(A;A) rs76454301(C;C) |
| Reference | Rs76454301(G;G) |
| Significance | Untested |
| Disease | Analbuminemia |
| Variation | info |
| Gene | ALB |
| CLNDBN | Analbuminemia |
| Reversed | 0 |
| HGVS | NC_000004.11:g.74277713G>A |
| CLNSRC | ClinVar |
| CLNACC | RCV000144407.1, |
[PMID 7937781
] Analbuminemia: three cases resulting from different point mutations in the albumin gene.
