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rs80259813

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs80259813(A;A)
Make rs80259813(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position73418166
GeneALB
is asnp
is mentioned by
dbSNPrs80259813
ebirs80259813
HLIrs80259813
Exacrs80259813
Varsomers80259813
Maprs80259813
PheGenIrs80259813
hapmaprs80259813
1000 genomesrs80259813
hgdprs80259813
ensemblrs80259813
gopubmedrs80259813
geneviewrs80259813
scholarrs80259813
googlers80259813
pharmgkbrs80259813
gwascentralrs80259813
openSNPrs80259813
23andMers80259813
23andMe allrs80259813
SNP Nexus

SNPshotrs80259813
SNPdbers80259813
MSV3drs80259813
GWAS Ctlgrs80259813
Max Magnitude0
OMIM103600
Desc
Variant0053
Relatedalso
ClinVar
Risk rs80259813(A;A)
Alt rs80259813(A;A)
Reference rs80259813(G;G)
Significance Other
Disease ALBUMIN DUBLIN
Variation info
Gene ALB
CLNDBN ALBUMIN DUBLIN
Reversed 0
HGVS NC_000004.11:g.74283883G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019897.1,


[PMID 1819460] Purification and structural study of two albumin variants in an Irish population.