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rs141733599

From SNPedia

Orientationplus
Stabilizedplus
Make rs141733599(C;C)
Make rs141733599(C;T)
Make rs141733599(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position73404406
GeneALB
is asnp
is mentioned by
dbSNPrs141733599
dbSNP (old)rs141733599
ClinGenrs141733599
ebirs141733599
HLIrs141733599
Exacrs141733599
Varsomers141733599
Maprs141733599
PheGenIrs141733599
Biobankrs141733599
1000 genomesrs141733599
hgdprs141733599
ensemblrs141733599
gopubmedrs141733599
geneviewrs141733599
scholarrs141733599
googlers141733599
pharmgkbrs141733599
gwascentralrs141733599
openSNPrs141733599
23andMers141733599
23andMe allrs141733599
SNP Nexus

SNPshotrs141733599
SNPdbers141733599
MSV3drs141733599
GWAS Ctlgrs141733599
Merged fromRs78611306
Max Magnitude
ClinVar
Risk rs141733599(T;T)
Alt rs141733599(T;T)
Reference rs141733599(C;C)
Significance Other
Disease ALBUMIN LARINO
Variation info
Gene ALB
CLNDBN ALBUMIN LARINO
Reversed 0
HGVS NC_000004.11:g.74270123C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019887.2,


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