rs77050410
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs77050410(A;A) |
Make rs77050410(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 73406741 |
Gene | ALB |
is a | snp |
is | mentioned by |
dbSNP | rs77050410 |
dbSNP (classic) | rs77050410 |
ClinGen | rs77050410 |
ebi | rs77050410 |
HLI | rs77050410 |
Exac | rs77050410 |
Gnomad | rs77050410 |
Varsome | rs77050410 |
LitVar | rs77050410 |
Map | rs77050410 |
PheGenI | rs77050410 |
Biobank | rs77050410 |
1000 genomes | rs77050410 |
hgdp | rs77050410 |
ensembl | rs77050410 |
geneview | rs77050410 |
scholar | rs77050410 |
rs77050410 | |
pharmgkb | rs77050410 |
gwascentral | rs77050410 |
openSNP | rs77050410 |
23andMe | rs77050410 |
SNPshot | rs77050410 |
SNPdbe | rs77050410 |
MSV3d | rs77050410 |
GWAS Ctlg | rs77050410 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs77050410(A;A) |
Alt | rs77050410(A;A) |
Reference | Rs77050410(G;G) |
Significance | Other |
Disease | ALBUMIN TORINO |
Variation | info |
Gene | ALB |
CLNDBN | ALBUMIN TORINO |
Reversed | 0 |
HGVS | NC_000004.11:g.74272458G>A |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000019878.1, |
[PMID 2247440] Mutations in genetic variants of human serum albumin found in Italy.