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rs75738598

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs75738598(A;C)
Make rs75738598(C;C)
ReferenceGRCh38 38.1/141
Chromosome4
Position73420262
GeneALB
is asnp
is mentioned by
dbSNPrs75738598
ebirs75738598
HLIrs75738598
Exacrs75738598
Varsomers75738598
Maprs75738598
PheGenIrs75738598
hapmaprs75738598
1000 genomesrs75738598
hgdprs75738598
ensemblrs75738598
gopubmedrs75738598
geneviewrs75738598
scholarrs75738598
googlers75738598
pharmgkbrs75738598
gwascentralrs75738598
openSNPrs75738598
23andMers75738598
23andMe allrs75738598
SNP Nexus

SNPshotrs75738598
SNPdbers75738598
MSV3drs75738598
GWAS Ctlgrs75738598
Max Magnitude0
OMIM103600
Desc
Variant0026
Relatedalso
ClinVar
Risk rs75738598(C,T;C,T)
Alt rs75738598(C,T;C,T)
Reference rs75738598(A;A)
Significance Other
Disease ALBUMIN VANVES
Variation info
Gene ALB
CLNDBN ALBUMIN VANVES
Reversed 0
HGVS NC_000004.12:g.73420262A>Y
CLNSRC OMIM Allelic Variant
CLNACC RCV000019868.1,


[PMID 3689800] Structural characterization of two genetic variants of human serum albumin.