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rs79228041

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs79228041(A;A)
Make rs79228041(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position73419634
GeneALB
is asnp
is mentioned by
dbSNPrs79228041
ebirs79228041
HLIrs79228041
Exacrs79228041
Varsomers79228041
Maprs79228041
PheGenIrs79228041
hapmaprs79228041
1000 genomesrs79228041
hgdprs79228041
ensemblrs79228041
gopubmedrs79228041
geneviewrs79228041
scholarrs79228041
googlers79228041
pharmgkbrs79228041
gwascentralrs79228041
openSNPrs79228041
23andMers79228041
23andMe allrs79228041
SNP Nexus

SNPshotrs79228041
SNPdbers79228041
MSV3drs79228041
GWAS Ctlgrs79228041
Max Magnitude0
OMIM103600
Desc
Variant0024
Relatedalso
ClinVar
Risk rs79228041(A;A)
Alt rs79228041(A;A)
Reference rs79228041(G;G)
Significance Pathogenic
Disease ALBUMIN B
Variation info
Gene ALB
CLNDBN ALBUMIN B
Reversed 0
HGVS NC_000004.11:g.74285351G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019862.25,


[PMID 3689800] Structural characterization of two genetic variants of human serum albumin.

[PMID 5059895] Amino acid substitution in two identical inherited human serum albumin variants: albumin Oliphant and albumin Ann Arbor.

[PMID 15680241] Effect of genetic variation on the thermal stability of human serum albumin.

[PMID 21499247OA-icon.png] Exome sequencing identifies GRIN2A as frequently mutated in melanoma.