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rs78538497

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs78538497(A;T)
Make rs78538497(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position73415142
GeneALB
is asnp
is mentioned by
dbSNPrs78538497
ebirs78538497
HLIrs78538497
Exacrs78538497
Varsomers78538497
Maprs78538497
PheGenIrs78538497
hapmaprs78538497
1000 genomesrs78538497
hgdprs78538497
ensemblrs78538497
gopubmedrs78538497
geneviewrs78538497
scholarrs78538497
googlers78538497
pharmgkbrs78538497
gwascentralrs78538497
openSNPrs78538497
23andMers78538497
23andMe allrs78538497
SNP Nexus

SNPshotrs78538497
SNPdbers78538497
MSV3drs78538497
GWAS Ctlgrs78538497
Max Magnitude0
OMIM103600
Desc
Variant0036
Relatedalso
ClinVar
Risk rs78538497(T;T)
Alt rs78538497(T;T)
Reference rs78538497(A;A)
Significance Other
Disease ALBUMIN IOWA CITY 1
Variation info
Gene ALB
CLNDBN ALBUMIN IOWA CITY 1
Reversed 0
HGVS NC_000004.11:g.74280859A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019881.1,


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