rs6028

Orientation

plus

Stabilized

plus

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

Make rs6028(C;C)

Make rs6028(C;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

169582444

Gene

F5

is a	snp
is	mentioned by
dbSNP	rs6028
dbSNP (classic)	rs6028
ClinGen	rs6028
ebi	rs6028
HLI	rs6028
Exac	rs6028
Gnomad	rs6028
Varsome	rs6028
LitVar	rs6028
Map	rs6028
PheGenI	rs6028
Biobank	rs6028
1000 genomes	rs6028
hgdp	rs6028
ensembl	rs6028
geneview	rs6028
scholar	rs6028
google	rs6028
pharmgkb	rs6028
gwascentral	rs6028
openSNP	rs6028
23andMe	rs6028
SNPshot	rs6028
SNPdbe	rs6028
MSV3d	rs6028
GWAS Ctlg	rs6028

GMAF

0.2282

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 22703881]
Trait
Title	Genetic Associations for Activated Partial Thromboplastin Time and Prothrombin Time, their Gene Expression Profiles, and Risk of Coronary Artery Disease.
Risk Allele	C
P-val	3E-9
Odds Ratio	0.2260 None

[PMID 18426996] Relations of inflammatory biomarkers and common genetic variants with arterial stiffness and wave reflection.

[PMID 19404301] Variation in the upstream region of P-Selectin (SELP) is a risk factor for SLE.

ClinVar
Risk	rs6028(C;C)
Alt	rs6028(C;C)
Reference	Rs6028(T;T)
Significance	Probable-non-pathogenic
Disease	not specified Thrombophilia Thrombophilia due to activated protein C resistance Factor V deficiency Budd-Chiari syndrome
Variation	info
Gene	F5
CLNDBN	not specified Thrombophilia Thrombophilia due to activated protein C resistance Factor V deficiency Budd-Chiari syndrome
Reversed	0
HGVS	NC_000001.10:g.169551682T>C
CLNSRC
CLNACC	RCV000243137.1, RCV000271943.1, RCV000311703.1, RCV000327005.1, RCV000366465.1,