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rs76587671

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs76587671(A;A)
Make rs76587671(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position73419613
GeneALB
is asnp
is mentioned by
dbSNPrs76587671
ebirs76587671
HLIrs76587671
Exacrs76587671
Varsomers76587671
Maprs76587671
PheGenIrs76587671
hapmaprs76587671
1000 genomesrs76587671
hgdprs76587671
ensemblrs76587671
gopubmedrs76587671
geneviewrs76587671
scholarrs76587671
googlers76587671
pharmgkbrs76587671
gwascentralrs76587671
openSNPrs76587671
23andMers76587671
23andMe allrs76587671
SNP Nexus

SNPshotrs76587671
SNPdbers76587671
MSV3drs76587671
GWAS Ctlgrs76587671
Max Magnitude0
OMIM103600
Desc
Variant0022
Relatedalso
ClinVar
Risk rs76587671(A;A)
Alt rs76587671(A;A)
Reference rs76587671(G;G)
Significance Other
Disease ALBUMIN FUKUOKA 1
Variation info
Gene ALB
CLNDBN ALBUMIN FUKUOKA 1
Reversed 0
HGVS NC_000004.11:g.74285330G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019858.1,


[PMID 2404284OA-icon.png] Point substitutions in albumin genetic variants from Asia.


[PMID 9392528] Effect of genetic variation on the fatty acid-binding properties of human serum albumin and proalbumin.