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rs78340021

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs78340021(G;T)
Make rs78340021(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position73412084
GeneALB
is asnp
is mentioned by
dbSNPrs78340021
ebirs78340021
HLIrs78340021
Exacrs78340021
Varsomers78340021
Maprs78340021
PheGenIrs78340021
hapmaprs78340021
1000 genomesrs78340021
hgdprs78340021
ensemblrs78340021
gopubmedrs78340021
geneviewrs78340021
scholarrs78340021
googlers78340021
pharmgkbrs78340021
gwascentralrs78340021
openSNPrs78340021
23andMers78340021
23andMe allrs78340021
SNP Nexus

SNPshotrs78340021
SNPdbers78340021
MSV3drs78340021
GWAS Ctlgrs78340021
Max Magnitude0
ClinVar
Risk rs78340021(T;T)
Alt rs78340021(T;T)
Reference rs78340021(G;G)
Significance Untested
Disease Analbuminemia
Variation info
Gene ALB
CLNDBN Analbuminemia
Reversed 0
HGVS NC_000004.11:g.74277801G>T
CLNSRC ClinVar
CLNACC RCV000144408.1,


[PMID 15613718] Novel nonsense mutation causes analbuminemia in a Moroccan family.