rs561241

Orientation

minus

Stabilized

minus

Make rs561241(A;A)

Make rs561241(A;G)

Make rs561241(G;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

113105720

Gene

F7

is a	snp
is	mentioned by
dbSNP	rs561241
dbSNP (classic)	rs561241
ClinGen	rs561241
ebi	rs561241
HLI	rs561241
Exac	rs561241
Gnomad	rs561241
Varsome	rs561241
LitVar	rs561241
Map	rs561241
PheGenI	rs561241
Biobank	rs561241
1000 genomes	rs561241
hgdp	rs561241
ensembl	rs561241
geneview	rs561241
scholar	rs561241
google	rs561241
pharmgkb	rs561241
gwascentral	rs561241
openSNP	rs561241
23andMe	rs561241
SNPshot	rs561241
SNPdbe	rs561241
MSV3d	rs561241
GWAS Ctlg	rs561241

GMAF

0.1028

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

[PMID 17903294] risk of cardiovascular disease

rs561241 for hemostatic factors was p = 4.5*10(-16)

[PMID 17903291] The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports.

[PMID 19474294] Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.

[PMID 19822575] Molecular interactions between HNF4a, FOXA2 and GABP identified at regulatory DNA elements through ChIP-sequencing.

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	4E-56
Odds Ratio	0.0350 None