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rs77645174

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs77645174(A;G)
Make rs77645174(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position73419532
GeneALB
is asnp
is mentioned by
dbSNPrs77645174
ebirs77645174
HLIrs77645174
Exacrs77645174
Varsomers77645174
Maprs77645174
PheGenIrs77645174
hapmaprs77645174
1000 genomesrs77645174
hgdprs77645174
ensemblrs77645174
gopubmedrs77645174
geneviewrs77645174
scholarrs77645174
googlers77645174
pharmgkbrs77645174
gwascentralrs77645174
openSNPrs77645174
23andMers77645174
23andMe allrs77645174
SNP Nexus

SNPshotrs77645174
SNPdbers77645174
MSV3drs77645174
GWAS Ctlgrs77645174
Max Magnitude0
OMIM103600
Desc
Variant0029
Relatedalso
ClinVar
Risk rs77645174(G;G)
Alt rs77645174(G;G)
Reference rs77645174(A;A)
Significance Other
Disease ALBUMIN CASTEL DI SANGRO
Variation info
Gene ALB
CLNDBN ALBUMIN CASTEL DI SANGRO
Reversed 0
HGVS NC_000004.11:g.74285249A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019871.1,


[PMID 1973054] The molecular defect of albumin Castel di Sangro: 536 Lys----Glu.