rs4524

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs4524(A;G)

Make rs4524(G;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

169542517

Gene

F5

is a	snp
is	mentioned by
dbSNP	rs4524
dbSNP (classic)	rs4524
ClinGen	rs4524
ebi	rs4524
HLI	rs4524
Exac	rs4524
Gnomad	rs4524
Varsome	rs4524
LitVar	rs4524
Map	rs4524
PheGenI	rs4524
Biobank	rs4524
1000 genomes	rs4524
hgdp	rs4524
ensembl	rs4524
geneview	rs4524
scholar	rs4524
google	rs4524
pharmgkb	rs4524
gwascentral	rs4524
openSNP	rs4524
23andMe	rs4524
SNPshot	rs4524
SNPdbe	rs4524
MSV3d	rs4524
GWAS Ctlg	rs4524

GMAF

0.2438

Max Magnitude

0

?

(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 20031567 ] 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,