Have questions? Visit https://www.reddit.com/r/SNPedia

rs78611306

From SNPedia

Merged intors141733599
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs78611306(C;C)
Make rs78611306(C;T)
Make rs78611306(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position73404406
GeneALB
is asnp
is mentioned by
dbSNPrs78611306
ebirs78611306
HLIrs78611306
Exacrs78611306
Varsomers78611306
Maprs78611306
PheGenIrs78611306
hapmaprs78611306
1000 genomesrs78611306
hgdprs78611306
ensemblrs78611306
gopubmedrs78611306
geneviewrs78611306
scholarrs78611306
googlers78611306
pharmgkbrs78611306
gwascentralrs78611306
openSNPrs78611306
23andMers78611306
23andMe allrs78611306
SNP Nexus

SNPshotrs78611306
SNPdbers78611306
MSV3drs78611306
GWAS Ctlgrs78611306
StatusMerged into rs141733599
Max Magnitude0
OMIM103600
Desc
Variant0042
Relatedalso
ClinVar
Risk rs78611306(C,T;C,T)
Alt rs78611306(C,T;C,T)
Reference rs78611306(G;G)
Significance Untested
Disease
Variation info
Gene ALB
CLNDBN
Reversed 0
HGVS NC_000004.11:g.74270832G>C
CLNSRC
CLNACC


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