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rs75920790

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs75920790(A;A)
Make rs75920790(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position73418211
GeneALB
is asnp
is mentioned by
dbSNPrs75920790
ebirs75920790
HLIrs75920790
Exacrs75920790
Varsomers75920790
Maprs75920790
PheGenIrs75920790
hapmaprs75920790
1000 genomesrs75920790
hgdprs75920790
ensemblrs75920790
gopubmedrs75920790
geneviewrs75920790
scholarrs75920790
googlers75920790
pharmgkbrs75920790
gwascentralrs75920790
openSNPrs75920790
23andMers75920790
23andMe allrs75920790
SNP Nexus

SNPshotrs75920790
SNPdbers75920790
MSV3drs75920790
GWAS Ctlgrs75920790
Max Magnitude0
OMIM103600
Desc
Variant0035
Relatedalso
ClinVar
Risk rs75920790(A;A)
Alt rs75920790(A;A)
Reference rs75920790(G;G)
Significance Other
Disease ALBUMIN CASEBROOK
Variation info
Gene ALB
CLNDBN ALBUMIN CASEBROOK
Reversed 0
HGVS NC_000004.11:g.74283928G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019880.1,


[PMID 1859851] Structural characterization of a glycoprotein variant of human serum albumin: albumin Casebrook (494 Asp----Asn).


[PMID 9392528] Effect of genetic variation on the fatty acid-binding properties of human serum albumin and proalbumin.