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rs80002911

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs80002911(A;G)
Make rs80002911(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position73413451
GeneALB
is asnp
is mentioned by
dbSNPrs80002911
ebirs80002911
HLIrs80002911
Exacrs80002911
Varsomers80002911
Maprs80002911
PheGenIrs80002911
hapmaprs80002911
1000 genomesrs80002911
hgdprs80002911
ensemblrs80002911
gopubmedrs80002911
geneviewrs80002911
scholarrs80002911
googlers80002911
pharmgkbrs80002911
gwascentralrs80002911
openSNPrs80002911
23andMers80002911
23andMe allrs80002911
SNP Nexus

SNPshotrs80002911
SNPdbers80002911
MSV3drs80002911
GWAS Ctlgrs80002911
Max Magnitude0
OMIM103600
Desc
Variant0049
Relatedalso
ClinVar
Risk rs80002911(G;G)
Alt rs80002911(G;G)
Reference rs80002911(A;A)
Significance Other
Disease ALBUMIN MALMO-10
Variation info
Gene ALB
CLNDBN ALBUMIN MALMO-10
Reversed 0
HGVS NC_000004.11:g.74279168A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019893.2,


[PMID 1518850OA-icon.png] Alloalbuminemia in Sweden: structural study and phenotypic distribution of nine albumin variants.