rs80296402
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs80296402(A;A) |
Make rs80296402(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 73408639 |
Gene | ALB |
is a | snp |
is | mentioned by |
dbSNP | rs80296402 |
dbSNP (classic) | rs80296402 |
ClinGen | rs80296402 |
ebi | rs80296402 |
HLI | rs80296402 |
Exac | rs80296402 |
Gnomad | rs80296402 |
Varsome | rs80296402 |
LitVar | rs80296402 |
Map | rs80296402 |
PheGenI | rs80296402 |
Biobank | rs80296402 |
1000 genomes | rs80296402 |
hgdp | rs80296402 |
ensembl | rs80296402 |
geneview | rs80296402 |
scholar | rs80296402 |
rs80296402 | |
pharmgkb | rs80296402 |
gwascentral | rs80296402 |
openSNP | rs80296402 |
23andMe | rs80296402 |
SNPshot | rs80296402 |
SNPdbe | rs80296402 |
MSV3d | rs80296402 |
GWAS Ctlg | rs80296402 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs80296402(A;A) |
Alt | rs80296402(A;A) |
Reference | Rs80296402(G;G) |
Significance | Other |
Disease | ALBUMIN VIBO VALENTIA |
Variation | info |
Gene | ALB |
CLNDBN | ALBUMIN VIBO VALENTIA |
Reversed | 0 |
HGVS | NC_000004.11:g.74274356G>A |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000019879.1, |
[PMID 2247440] Mutations in genetic variants of human serum albumin found in Italy.