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rs74826639

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs74826639(A;A)
Make rs74826639(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position73418244
GeneALB
is asnp
is mentioned by
dbSNPrs74826639
ebirs74826639
HLIrs74826639
Exacrs74826639
Varsomers74826639
Maprs74826639
PheGenIrs74826639
hapmaprs74826639
1000 genomesrs74826639
hgdprs74826639
ensemblrs74826639
gopubmedrs74826639
geneviewrs74826639
scholarrs74826639
googlers74826639
pharmgkbrs74826639
gwascentralrs74826639
openSNPrs74826639
23andMers74826639
23andMe allrs74826639
SNP Nexus

SNPshotrs74826639
SNPdbers74826639
MSV3drs74826639
GWAS Ctlgrs74826639
Max Magnitude0
OMIM103600
Desc
Variant0054
Relatedalso
ClinVar
Risk rs74826639(A;A)
Alt rs74826639(A;A)
Reference rs74826639(G;G)
Significance Other
Disease ALBUMIN ORTONOVO
Variation info
Gene ALB
CLNDBN ALBUMIN ORTONOVO
Reversed 0
HGVS NC_000004.11:g.74283961G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019898.1,


[PMID 7902134] Protein and DNA sequence analysis of a 'private' genetic variant: albumin Ortonovo (Glu-505-->Lys).