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rs80296402

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs80296402(A;A)
Make rs80296402(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position73408639
GeneALB
is asnp
is mentioned by
dbSNPrs80296402
ebirs80296402
HLIrs80296402
Exacrs80296402
Varsomers80296402
Maprs80296402
PheGenIrs80296402
hapmaprs80296402
1000 genomesrs80296402
hgdprs80296402
ensemblrs80296402
gopubmedrs80296402
geneviewrs80296402
scholarrs80296402
googlers80296402
pharmgkbrs80296402
gwascentralrs80296402
openSNPrs80296402
23andMers80296402
23andMe allrs80296402
SNP Nexus

SNPshotrs80296402
SNPdbers80296402
MSV3drs80296402
GWAS Ctlgrs80296402
Max Magnitude0
OMIM103600
Desc
Variant0034
Relatedalso
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
CLNACC RCV000019879.1,


[PMID 2247440OA-icon.png] Mutations in genetic variants of human serum albumin found in Italy.