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rs80106970

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80106970(A;G)
Make rs80106970(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position73420257
GeneALB
is asnp
is mentioned by
dbSNPrs80106970
ebirs80106970
HLIrs80106970
Exacrs80106970
Varsomers80106970
Maprs80106970
PheGenIrs80106970
hapmaprs80106970
1000 genomesrs80106970
hgdprs80106970
ensemblrs80106970
gopubmedrs80106970
geneviewrs80106970
scholarrs80106970
googlers80106970
pharmgkbrs80106970
gwascentralrs80106970
openSNPrs80106970
23andMers80106970
23andMe allrs80106970
SNP Nexus

SNPshotrs80106970
SNPdbers80106970
MSV3drs80106970
GWAS Ctlgrs80106970
Max Magnitude0
OMIM103600
Desc
Variant0025
Relatedalso
ClinVar
Risk rs80106970(G;G)
Alt rs80106970(G;G)
Reference rs80106970(A;A)
Significance Non-pathogenic
Disease not specified
Variation info
Gene ALB
CLNDBN not specified
Reversed 0
HGVS NC_000004.11:g.74285974A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019867.2,


[PMID 3967761] Localization of the amino acid substitution site in a fast migrating variant of human serum albumin.

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