rs78283180
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs78283180(A;G) |
Make rs78283180(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 73409363 |
Gene | ALB |
is a | snp |
is | mentioned by |
dbSNP | rs78283180 |
dbSNP (classic) | rs78283180 |
ClinGen | rs78283180 |
ebi | rs78283180 |
HLI | rs78283180 |
Exac | rs78283180 |
Gnomad | rs78283180 |
Varsome | rs78283180 |
LitVar | rs78283180 |
Map | rs78283180 |
PheGenI | rs78283180 |
Biobank | rs78283180 |
1000 genomes | rs78283180 |
hgdp | rs78283180 |
ensembl | rs78283180 |
geneview | rs78283180 |
scholar | rs78283180 |
rs78283180 | |
pharmgkb | rs78283180 |
gwascentral | rs78283180 |
openSNP | rs78283180 |
23andMe | rs78283180 |
SNPshot | rs78283180 |
SNPdbe | rs78283180 |
MSV3d | rs78283180 |
GWAS Ctlg | rs78283180 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs78283180(G;G) |
Alt | rs78283180(G;G) |
Reference | Rs78283180(A;A) |
Significance | Other |
Disease | ALBUMIN ASOLA |
Variation | info |
Gene | ALB |
CLNDBN | ALBUMIN ASOLA |
Reversed | 0 |
HGVS | NC_000004.11:g.74275080A>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000019891.1, |
[PMID 7882997] A genetic variant of albumin (albumin Asola; Tyr140-->Cys) with no free -SH group but with an additional disulfide bridge.