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rs77892378

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs77892378(C;C)
Make rs77892378(C;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position73406760
GeneALB
is asnp
is mentioned by
dbSNPrs77892378
ebirs77892378
HLIrs77892378
Exacrs77892378
Varsomers77892378
Maprs77892378
PheGenIrs77892378
hapmaprs77892378
1000 genomesrs77892378
hgdprs77892378
ensemblrs77892378
gopubmedrs77892378
geneviewrs77892378
scholarrs77892378
googlers77892378
pharmgkbrs77892378
gwascentralrs77892378
openSNPrs77892378
23andMers77892378
23andMe allrs77892378
SNP Nexus

SNPshotrs77892378
SNPdbers77892378
MSV3drs77892378
GWAS Ctlgrs77892378
Max Magnitude0
OMIM103600
Desc
Variant0056
Relatedalso
ClinVar
Risk rs77892378(C,G;C,G)
Alt rs77892378(C,G;C,G)
Reference rs77892378(T;T)
Significance Other
Disease Hyperthyroxinemia
Variation info
Gene ALB
CLNDBN Hyperthyroxinemia, familial dysalbuminemic
Reversed 0
HGVS NC_000004.11:g.74272477T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000019900.29,


[PMID 9589637] Familial dysalbuminemic hypertriiodothyroninemia: a new, dominantly inherited albumin defect.