rs77656691
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs77656691(G;T) |
| Make rs77656691(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 73409474 |
| Gene | ALB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs77656691 |
| dbSNP (classic) | rs77656691 |
| ClinGen | rs77656691 |
| ebi | rs77656691 |
| HLI | rs77656691 |
| Exac | rs77656691 |
| Gnomad | rs77656691 |
| Varsome | rs77656691 |
| LitVar | rs77656691 |
| Map | rs77656691 |
| PheGenI | rs77656691 |
| Biobank | rs77656691 |
| 1000 genomes | rs77656691 |
| hgdp | rs77656691 |
| ensembl | rs77656691 |
| geneview | rs77656691 |
| scholar | rs77656691 |
| rs77656691 | |
| pharmgkb | rs77656691 |
| gwascentral | rs77656691 |
| openSNP | rs77656691 |
| 23andMe | rs77656691 |
| SNPshot | rs77656691 |
| SNPdbe | rs77656691 |
| MSV3d | rs77656691 |
| GWAS Ctlg | rs77656691 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs77656691(T;T) |
| Alt | rs77656691(T;T) |
| Reference | Rs77656691(G;G) |
| Significance | Other |
| Disease | ALBUMIN HAWKES BAY |
| Variation | info |
| Gene | ALB |
| CLNDBN | ALBUMIN HAWKES BAY |
| Reversed | 0 |
| HGVS | NC_000004.11:g.74275191G>T |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000019875.1, |
[PMID 8347685] Albumin Hawkes Bay; a low level variant caused by loss of a sulphydryl group at position 177.
