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rs79804069

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs79804069(A;C)
Make rs79804069(C;C)
ReferenceGRCh38 38.1/141
Chromosome4
Position73412027
GeneALB
is asnp
is mentioned by
dbSNPrs79804069
ebirs79804069
HLIrs79804069
Exacrs79804069
Varsomers79804069
Maprs79804069
PheGenIrs79804069
hapmaprs79804069
1000 genomesrs79804069
hgdprs79804069
ensemblrs79804069
gopubmedrs79804069
geneviewrs79804069
scholarrs79804069
googlers79804069
pharmgkbrs79804069
gwascentralrs79804069
openSNPrs79804069
23andMers79804069
23andMe allrs79804069
SNP Nexus

SNPshotrs79804069
SNPdbers79804069
MSV3drs79804069
GWAS Ctlgrs79804069
GMAF0.0004591
Max Magnitude0
OMIM103600
Desc
Variant0043
Relatedalso
ClinVar
Risk rs79804069(C,G;C,G)
Alt rs79804069(C,G;C,G)
Reference rs79804069(A;A)
Significance Other
Disease ALBUMIN TRADATE 2
Variation info
Gene ALB
CLNDBN ALBUMIN TRADATE 2
Reversed 0
HGVS NC_000004.11:g.74277744A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000019888.1,


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