rs78574148
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs78574148(A;A) |
| Make rs78574148(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 73406750 |
| Gene | ALB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs78574148 |
| dbSNP (classic) | rs78574148 |
| ClinGen | rs78574148 |
| ebi | rs78574148 |
| HLI | rs78574148 |
| Exac | rs78574148 |
| Gnomad | rs78574148 |
| Varsome | rs78574148 |
| LitVar | rs78574148 |
| Map | rs78574148 |
| PheGenI | rs78574148 |
| Biobank | rs78574148 |
| 1000 genomes | rs78574148 |
| hgdp | rs78574148 |
| ensembl | rs78574148 |
| geneview | rs78574148 |
| scholar | rs78574148 |
| rs78574148 | |
| pharmgkb | rs78574148 |
| gwascentral | rs78574148 |
| openSNP | rs78574148 |
| 23andMe | rs78574148 |
| SNPshot | rs78574148 |
| SNPdbe | rs78574148 |
| MSV3d | rs78574148 |
| GWAS Ctlg | rs78574148 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs78574148(A;A) |
| Alt | rs78574148(A;A) |
| Reference | Rs78574148(G;G) |
| Significance | Other |
| Disease | ALBUMIN MALMO-95 |
| Variation | info |
| Gene | ALB |
| CLNDBN | ALBUMIN MALMO-95 |
| Reversed | 0 |
| HGVS | NC_000004.11:g.74272467G>A |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000019892.2, |
[PMID 1518850
] Alloalbuminemia in Sweden: structural study and phenotypic distribution of nine albumin variants.
[PMID 2404284] Point substitutions in albumin genetic variants from Asia.
[PMID 15680241] Effect of genetic variation on the thermal stability of human serum albumin.
