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rs79738788

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs79738788(A;G)
Make rs79738788(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position73419575
GeneALB
is asnp
is mentioned by
dbSNPrs79738788
ebirs79738788
HLIrs79738788
Exacrs79738788
Varsomers79738788
Maprs79738788
PheGenIrs79738788
hapmaprs79738788
1000 genomesrs79738788
hgdprs79738788
ensemblrs79738788
gopubmedrs79738788
geneviewrs79738788
scholarrs79738788
googlers79738788
pharmgkbrs79738788
gwascentralrs79738788
openSNPrs79738788
23andMers79738788
23andMe allrs79738788
SNP Nexus

SNPshotrs79738788
SNPdbers79738788
MSV3drs79738788
GWAS Ctlgrs79738788
Max Magnitude0
OMIM103600
Desc
Variant0021
Relatedalso
ClinVar
Risk rs79738788(C,G;C,G)
Alt rs79738788(C,G;C,G)
Reference rs79738788(A;A)
Significance Other
Disease Alloalbuminemia ALBUMIN MEXICO 2
Variation info
Gene ALB
CLNDBN Alloalbuminemia ALBUMIN MEXICO 2
Reversed 0
HGVS NC_000004.11:g.74285292A>C; NC_000004.11:g.74285292A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000144399.1, RCV000019857.1,


[PMID 3474609OA-icon.png] Amino acid substitutions in genetic variants of human serum albumin and in sequences inferred from molecular cloning.


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