rs74826639
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs74826639(A;A) |
Make rs74826639(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 73418244 |
Gene | ALB |
is a | snp |
is | mentioned by |
dbSNP | rs74826639 |
dbSNP (classic) | rs74826639 |
ClinGen | rs74826639 |
ebi | rs74826639 |
HLI | rs74826639 |
Exac | rs74826639 |
Gnomad | rs74826639 |
Varsome | rs74826639 |
LitVar | rs74826639 |
Map | rs74826639 |
PheGenI | rs74826639 |
Biobank | rs74826639 |
1000 genomes | rs74826639 |
hgdp | rs74826639 |
ensembl | rs74826639 |
geneview | rs74826639 |
scholar | rs74826639 |
rs74826639 | |
pharmgkb | rs74826639 |
gwascentral | rs74826639 |
openSNP | rs74826639 |
23andMe | rs74826639 |
SNPshot | rs74826639 |
SNPdbe | rs74826639 |
MSV3d | rs74826639 |
GWAS Ctlg | rs74826639 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs74826639(A;A) |
Alt | rs74826639(A;A) |
Reference | Rs74826639(G;G) |
Significance | Other |
Disease | ALBUMIN ORTONOVO |
Variation | info |
Gene | ALB |
CLNDBN | ALBUMIN ORTONOVO |
Reversed | 0 |
HGVS | NC_000004.11:g.74283961G>A |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000019898.1, |
[PMID 7902134] Protein and DNA sequence analysis of a 'private' genetic variant: albumin Ortonovo (Glu-505-->Lys).