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rs77354753

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs77354753(A;A)
Make rs77354753(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position73415045
GeneALB
is asnp
is mentioned by
dbSNPrs77354753
ebirs77354753
HLIrs77354753
Exacrs77354753
Varsomers77354753
Maprs77354753
PheGenIrs77354753
hapmaprs77354753
1000 genomesrs77354753
hgdprs77354753
ensemblrs77354753
gopubmedrs77354753
geneviewrs77354753
scholarrs77354753
googlers77354753
pharmgkbrs77354753
gwascentralrs77354753
openSNPrs77354753
23andMers77354753
23andMe allrs77354753
SNP Nexus

SNPshotrs77354753
SNPdbers77354753
MSV3drs77354753
GWAS Ctlgrs77354753
Max Magnitude0
OMIM103600
Desc
Variant0051
Relatedalso
ClinVar
Risk rs77354753(A;A)
Alt rs77354753(A;A)
Reference rs77354753(G;G)
Significance Other
Disease ALBUMIN SONDRIA
Variation info
Gene ALB
CLNDBN ALBUMIN SONDRIA
Reversed 0
HGVS NC_000004.11:g.74280762G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019895.1,


[PMID 1347703] Two alloalbumins with identical electrophoretic mobility are produced by differently charged amino acid substitutions.