rs75470261
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs75470261(C;T) |
| Make rs75470261(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 73406657 |
| Gene | ALB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs75470261 |
| dbSNP (classic) | rs75470261 |
| ClinGen | rs75470261 |
| ebi | rs75470261 |
| HLI | rs75470261 |
| Exac | rs75470261 |
| Gnomad | rs75470261 |
| Varsome | rs75470261 |
| LitVar | rs75470261 |
| Map | rs75470261 |
| PheGenI | rs75470261 |
| Biobank | rs75470261 |
| 1000 genomes | rs75470261 |
| hgdp | rs75470261 |
| ensembl | rs75470261 |
| geneview | rs75470261 |
| scholar | rs75470261 |
| rs75470261 | |
| pharmgkb | rs75470261 |
| gwascentral | rs75470261 |
| openSNP | rs75470261 |
| 23andMe | rs75470261 |
| SNPshot | rs75470261 |
| SNPdbe | rs75470261 |
| MSV3d | rs75470261 |
| GWAS Ctlg | rs75470261 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs75470261(T;T) |
| Alt | rs75470261(T;T) |
| Reference | Rs75470261(C;C) |
| Significance | Untested |
| Disease | Analbuminemia |
| Variation | info |
| Gene | ALB |
| CLNDBN | Analbuminemia |
| Reversed | 0 |
| HGVS | NC_000004.11:g.74272374C>T |
| CLNSRC | ClinVar |
| CLNACC | RCV000144398.1, |
[PMID 7937781
] Analbuminemia: three cases resulting from different point mutations in the albumin gene.
