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rs5110

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs5110(G;T)
Make rs5110(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position116820918
GeneAPOA4
is asnp
is mentioned by
dbSNPrs5110
dbSNP (classic)rs5110
ClinGenrs5110
ebirs5110
HLIrs5110
Exacrs5110
Gnomadrs5110
Varsomers5110
LitVarrs5110
Maprs5110
PheGenIrs5110
Biobankrs5110
1000 genomesrs5110
hgdprs5110
ensemblrs5110
geneviewrs5110
scholarrs5110
googlers5110
pharmgkbrs5110
gwascentralrs5110
openSNPrs5110
23andMers5110
SNPshotrs5110
SNPdbers5110
MSV3drs5110
GWAS Ctlgrs5110
GMAF0.03306
Max Magnitude0
? (G;G) (G;T) (T;T) 28


OMIM107690
Desc
Variant0001
Relatedalso


ClinVar
Risk rs5110(T;T)
Alt rs5110(T;T)
Reference Rs5110(G;G)
Significance Pathogenic
Disease APOLIPOPROTEIN A-IV POLYMORPHISM
Variation info
Gene APOA4
CLNDBN APOLIPOPROTEIN A-IV POLYMORPHISM, APOA4*1/APOA4*2
Reversed 1
HGVS NC_000011.9:g.116691634C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019494.2,



The apolipoprotein A-IV polymorphism rs5110 is also known as c.1140G>T, p.Gln380His and Q360H.


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[PMID 19263529OA-icon.png] Genetic risk factors in recurrent venous thromboembolism: A multilocus, population-based, prospective approach.