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rs80095457

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs80095457(A;G)
Make rs80095457(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position73408778
GeneALB
is asnp
is mentioned by
dbSNPrs80095457
ebirs80095457
HLIrs80095457
Exacrs80095457
Varsomers80095457
Maprs80095457
PheGenIrs80095457
hapmaprs80095457
1000 genomesrs80095457
hgdprs80095457
ensemblrs80095457
gopubmedrs80095457
geneviewrs80095457
scholarrs80095457
googlers80095457
pharmgkbrs80095457
gwascentralrs80095457
openSNPrs80095457
23andMers80095457
23andMe allrs80095457
SNP Nexus

SNPshotrs80095457
SNPdbers80095457
MSV3drs80095457
GWAS Ctlgrs80095457
Max Magnitude0
OMIM103600
Desc
Variant0037
Relatedalso
ClinVar
Risk rs80095457(G;G)
Alt rs80095457(G;G)
Reference rs80095457(A;A)
Significance Other
Disease ALBUMIN KOMAGOME 2
Variation info
Gene ALB
CLNDBN ALBUMIN KOMAGOME 2
Reversed 0
HGVS NC_000004.11:g.74274495A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019882.1,


[PMID 1946412OA-icon.png] Genetic variants of serum albumin in Americans and Japanese.