rs76587671
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs76587671(A;A) |
| Make rs76587671(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 73419613 |
| Gene | ALB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs76587671 |
| dbSNP (classic) | rs76587671 |
| ClinGen | rs76587671 |
| ebi | rs76587671 |
| HLI | rs76587671 |
| Exac | rs76587671 |
| Gnomad | rs76587671 |
| Varsome | rs76587671 |
| LitVar | rs76587671 |
| Map | rs76587671 |
| PheGenI | rs76587671 |
| Biobank | rs76587671 |
| 1000 genomes | rs76587671 |
| hgdp | rs76587671 |
| ensembl | rs76587671 |
| geneview | rs76587671 |
| scholar | rs76587671 |
| rs76587671 | |
| pharmgkb | rs76587671 |
| gwascentral | rs76587671 |
| openSNP | rs76587671 |
| 23andMe | rs76587671 |
| SNPshot | rs76587671 |
| SNPdbe | rs76587671 |
| MSV3d | rs76587671 |
| GWAS Ctlg | rs76587671 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs76587671(A;A) |
| Alt | rs76587671(A;A) |
| Reference | Rs76587671(G;G) |
| Significance | Other |
| Disease | ALBUMIN FUKUOKA 1 |
| Variation | info |
| Gene | ALB |
| CLNDBN | ALBUMIN FUKUOKA 1 |
| Reversed | 0 |
| HGVS | NC_000004.11:g.74285330G>A |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000019858.1, |
[PMID 2404284
] Point substitutions in albumin genetic variants from Asia.
[PMID 9392528] Effect of genetic variation on the fatty acid-binding properties of human serum albumin and proalbumin.
