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rs77158239

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs77158239(-;-)
Make rs77158239(-;C)
ReferenceGRCh38 38.1/141
Chromosome4
Position73420278
GeneALB
is asnp
is mentioned by
dbSNPrs77158239
ebirs77158239
HLIrs77158239
Exacrs77158239
Varsomers77158239
Maprs77158239
PheGenIrs77158239
hapmaprs77158239
1000 genomesrs77158239
hgdprs77158239
ensemblrs77158239
gopubmedrs77158239
geneviewrs77158239
scholarrs77158239
googlers77158239
pharmgkbrs77158239
gwascentralrs77158239
openSNPrs77158239
23andMers77158239
23andMe allrs77158239
SNP Nexus

SNPshotrs77158239
SNPdbers77158239
MSV3drs77158239
GWAS Ctlgrs77158239
Max Magnitude0
OMIM103600
Desc
Variant0032
Relatedalso
ClinVar
Risk
Alt
Reference Rs77158239(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene ALB
CLNDBN not specified
Reversed 0
HGVS NC_000004.11:g.74285995delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000019877.2,


[PMID 2068071OA-icon.png] A donor splice mutation and a single-base deletion produce two carboxyl-terminal variants of human serum albumin.


[PMID 3081519] Structural characterization of a chain termination mutant of human serum albumin.