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rs74674594

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs74674594(-;-)
Make rs74674594(-;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position73419625
GeneALB
is asnp
is mentioned by
dbSNPrs74674594
ebirs74674594
HLIrs74674594
Exacrs74674594
Varsomers74674594
Maprs74674594
PheGenIrs74674594
hapmaprs74674594
1000 genomesrs74674594
hgdprs74674594
ensemblrs74674594
gopubmedrs74674594
geneviewrs74674594
scholarrs74674594
googlers74674594
pharmgkbrs74674594
gwascentralrs74674594
openSNPrs74674594
23andMers74674594
23andMe allrs74674594
SNP Nexus

SNPshotrs74674594
SNPdbers74674594
MSV3drs74674594
GWAS Ctlgrs74674594
Max Magnitude0
OMIM103600
Desc
Variant0045
Relatedalso
ClinVar
Risk rs74674594(;)
Alt rs74674594(;)
Reference rs74674594(T;T)
Significance Other
Disease ALBUMIN BAZZANO
Variation info
Gene ALB
CLNDBN ALBUMIN BAZZANO
Reversed 0
HGVS NC_000004.11:g.74285342delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000019890.2,


[PMID 8022807OA-icon.png] Genetic variants of human serum albumin in Italy: point mutants and a carboxyl-terminal variant.


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