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rs76285851

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs76285851(A;A)
Make rs76285851(A;C)
ReferenceGRCh38 38.1/141
Chromosome4
Position73405117
GeneALB
is asnp
is mentioned by
dbSNPrs76285851
ebirs76285851
HLIrs76285851
Exacrs76285851
Varsomers76285851
Maprs76285851
PheGenIrs76285851
hapmaprs76285851
1000 genomesrs76285851
hgdprs76285851
ensemblrs76285851
gopubmedrs76285851
geneviewrs76285851
scholarrs76285851
googlers76285851
pharmgkbrs76285851
gwascentralrs76285851
openSNPrs76285851
23andMers76285851
23andMe allrs76285851
SNP Nexus

SNPshotrs76285851
SNPdbers76285851
MSV3drs76285851
GWAS Ctlgrs76285851
Max Magnitude0
OMIM103600
Desc
Variant0005
Relatedalso
ClinVar
Risk rs76285851(A,G;A,G)
Alt rs76285851(A,G;A,G)
Reference rs76285851(C;C)
Significance Other
Disease ALBUMIN NAGASAKI 3
Variation info
Gene ALB
CLNDBN ALBUMIN NAGASAKI 3
Reversed 0
HGVS NC_000004.12:g.73405117C>R
CLNSRC OMIM Allelic Variant
CLNACC RCV000019829.1,


[PMID 3478700OA-icon.png] Structural changes and metal binding by proalbumins and other amino-terminal genetic variants of human serum albumin.