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rs79744198

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs79744198(A;G)
Make rs79744198(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position73413454
GeneALB
is asnp
is mentioned by
dbSNPrs79744198
ebirs79744198
HLIrs79744198
Exacrs79744198
Varsomers79744198
Maprs79744198
PheGenIrs79744198
hapmaprs79744198
1000 genomesrs79744198
hgdprs79744198
ensemblrs79744198
gopubmedrs79744198
geneviewrs79744198
scholarrs79744198
googlers79744198
pharmgkbrs79744198
gwascentralrs79744198
openSNPrs79744198
23andMers79744198
23andMe allrs79744198
SNP Nexus

SNPshotrs79744198
SNPdbers79744198
MSV3drs79744198
GWAS Ctlgrs79744198
Max Magnitude0
OMIM103600
Desc
Variant0008
Relatedalso
ClinVar
Risk rs79744198(G;G)
Alt rs79744198(G;G)
Reference rs79744198(A;A)
Significance Non-pathogenic
Disease not specified
Variation info
Gene ALB
CLNDBN not specified
Reversed 0
HGVS NC_000004.11:g.74279171A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019833.2,


[PMID 2226433] Hormone binding to natural mutants of human serum albumin.

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

[PMID 3594916] The molecular abnormality of albumin Niigata: 269 Asp----Gly.