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rs4524

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs4524(A;G)
Make rs4524(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position169542517
GeneF5
is asnp
is mentioned by
dbSNPrs4524
dbSNP (classic)rs4524
ClinGenrs4524
ebirs4524
HLIrs4524
Exacrs4524
Gnomadrs4524
Varsomers4524
LitVarrs4524
Maprs4524
PheGenIrs4524
Biobankrs4524
1000 genomesrs4524
hgdprs4524
ensemblrs4524
geneviewrs4524
scholarrs4524
googlers4524
pharmgkbrs4524
gwascentralrs4524
openSNPrs4524
23andMers4524
SNPshotrs4524
SNPdbers4524
MSV3drs4524
GWAS Ctlgrs4524
GMAF0.2438
Max Magnitude0
? (A;A) (A;G) (G;G) 28


Gene variants associated with deep vein thrombosis.[PMID 18349091]

Updated analysis of gene variants associated with deep vein thrombosis.[PMID 20124536]


[PMID 20031567OA-icon.png] An evaluation of candidate genes of inflammation and thrombosis in relation to the risk of venous thromboembolism: The Women's Genome Health Study.


[PMID 22533697] Candidate gene polymorphisms and the risk for pregnancy-related venous thrombosis.



ClinVar
Risk rs4524(G;G)
Alt rs4524(G;G)
Reference Rs4524(A;A)
Significance Probable-non-pathogenic
Disease not specified Thrombophilia due to activated protein C resistance
Variation info
Gene F5
CLNDBN not specified Thrombophilia due to activated protein C resistance
Reversed 1
HGVS NC_000001.10:g.169511755T>C
CLNSRC
CLNACC RCV000242831.1, RCV000351409.1,