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rs79047363

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs79047363(A;A)
Make rs79047363(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position73416262
GeneALB
is asnp
is mentioned by
dbSNPrs79047363
ebirs79047363
HLIrs79047363
Exacrs79047363
Varsomers79047363
Maprs79047363
PheGenIrs79047363
hapmaprs79047363
1000 genomesrs79047363
hgdprs79047363
ensemblrs79047363
gopubmedrs79047363
geneviewrs79047363
scholarrs79047363
googlers79047363
pharmgkbrs79047363
gwascentralrs79047363
openSNPrs79047363
23andMers79047363
23andMe allrs79047363
SNP Nexus

SNPshotrs79047363
SNPdbers79047363
MSV3drs79047363
GWAS Ctlgrs79047363
Max Magnitude0
OMIM103600
Desc
Variant0017
Relatedalso
OMIM103600
Desc
Variant0052
Relatedalso
ClinVar
Risk rs79047363(A,C;A,C)
Alt rs79047363(A,C;A,C)
Reference rs79047363(G;G)
Significance Other
Disease ALBUMIN TOCHIGI ALBUMIN MALMO-5
Variation info
Gene ALB
CLNDBN ALBUMIN TOCHIGI ALBUMIN MALMO-5
Reversed 0
HGVS NC_000004.11:g.74281979G>A; NC_000004.11:g.74281979G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000019847.1, RCV000019896.2,


[PMID 2762316OA-icon.png] Point substitutions in Japanese alloalbumins.


[PMID 1518850OA-icon.png] Alloalbuminemia in Sweden: structural study and phenotypic distribution of nine albumin variants.