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rs77187142

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs77187142(C;C)
Make rs77187142(C;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position73415141
GeneALB
is asnp
is mentioned by
dbSNPrs77187142
ebirs77187142
HLIrs77187142
Exacrs77187142
Varsomers77187142
Maprs77187142
PheGenIrs77187142
hapmaprs77187142
1000 genomesrs77187142
hgdprs77187142
ensemblrs77187142
gopubmedrs77187142
geneviewrs77187142
scholarrs77187142
googlers77187142
pharmgkbrs77187142
gwascentralrs77187142
openSNPrs77187142
23andMers77187142
23andMe allrs77187142
SNP Nexus

SNPshotrs77187142
SNPdbers77187142
MSV3drs77187142
GWAS Ctlgrs77187142
Max Magnitude0
OMIM103600
Desc
Variant0014
Relatedalso
ClinVar
Risk rs77187142(C;C)
Alt rs77187142(C;C)
Reference rs77187142(G;G)
Significance Other
Disease ALBUMIN PARKLANDS
Variation info
Gene ALB
CLNDBN ALBUMIN PARKLANDS
Reversed 0
HGVS NC_000004.11:g.74280858G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000019842.1,


[PMID 2304452] Binding of warfarin, salicylate, and diazepam to genetic variants of human serum albumin with known mutations.


[PMID 4027254] The molecular abnormality of albumin Parklands: 365 Asp----His.