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rs74718349

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs74718349(C;C)
Make rs74718349(C;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position73413476
GeneALB
is asnp
is mentioned by
dbSNPrs74718349
ebirs74718349
HLIrs74718349
Exacrs74718349
Varsomers74718349
Maprs74718349
PheGenIrs74718349
hapmaprs74718349
1000 genomesrs74718349
hgdprs74718349
ensemblrs74718349
gopubmedrs74718349
geneviewrs74718349
scholarrs74718349
googlers74718349
pharmgkbrs74718349
gwascentralrs74718349
openSNPrs74718349
23andMers74718349
23andMe allrs74718349
SNP Nexus

SNPshotrs74718349
SNPdbers74718349
MSV3drs74718349
GWAS Ctlgrs74718349
Max Magnitude0
OMIM103600
Desc
Variant0044
Relatedalso
ClinVar
Risk rs74718349(C,T;C,T)
Alt rs74718349(C,T;C,T)
Reference rs74718349(G;G)
Significance Other
Disease ALBUMIN CASERTA
Variation info
Gene ALB
CLNDBN ALBUMIN CASERTA
Reversed 0
HGVS NC_000004.11:g.74279193G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000019889.1,


[PMID 8022807OA-icon.png] Genetic variants of human serum albumin in Italy: point mutants and a carboxyl-terminal variant.