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rs79377490

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs79377490(A;G)
Make rs79377490(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position73412072
GeneALB
is asnp
is mentioned by
dbSNPrs79377490
ebirs79377490
HLIrs79377490
Exacrs79377490
Varsomers79377490
Maprs79377490
PheGenIrs79377490
hapmaprs79377490
1000 genomesrs79377490
hgdprs79377490
ensemblrs79377490
gopubmedrs79377490
geneviewrs79377490
scholarrs79377490
googlers79377490
pharmgkbrs79377490
gwascentralrs79377490
openSNPrs79377490
23andMers79377490
23andMe allrs79377490
SNP Nexus

SNPshotrs79377490
SNPdbers79377490
MSV3drs79377490
GWAS Ctlgrs79377490
Max Magnitude0
OMIM103600
Desc
Variant0039
Relatedalso
ClinVar
Risk rs79377490(G;G)
Alt rs79377490(G;G)
Reference rs79377490(A;A)
Significance Other
Disease ALBUMIN HERBORN
Variation info
Gene ALB
CLNDBN ALBUMIN HERBORN
Reversed 0
HGVS NC_000004.11:g.74277789A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019884.1,


[PMID 8513793] The structural characterization and bilirubin-binding properties of albumin Herborn, a [Lys240-->Glu] albumin mutant.