rs5896

Orientation

plus

Stabilized

plus

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

Make rs5896(C;T)

Make rs5896(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

46723453

Gene

F2

is a	snp
is	mentioned by
dbSNP	rs5896
dbSNP (classic)	rs5896
ClinGen	rs5896
ebi	rs5896
HLI	rs5896
Exac	rs5896
Gnomad	rs5896
Varsome	rs5896
LitVar	rs5896
Map	rs5896
PheGenI	rs5896
Biobank	rs5896
1000 genomes	rs5896
hgdp	rs5896
ensembl	rs5896
geneview	rs5896
scholar	rs5896
google	rs5896
pharmgkb	rs5896
gwascentral	rs5896
openSNP	rs5896
23andMe	rs5896
SNPshot	rs5896
SNPdbe	rs5896
MSV3d	rs5896
GWAS Ctlg	rs5896

GMAF

0.2452

Max Magnitude

0

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

[PMID 24162564] Association between prothrombin gene polymorphisms and hereditary thrombophilia in Xinjiang Kazakhs population

[PMID 16255080] A haplotype map of the human genome.

[PMID 17048007] Association of warfarin dose with genes involved in its action and metabolism.

[PMID 18305455] Use of pharmacogenetic and clinical factors to predict the therapeutic dose of warfarin.

[PMID 18596683] Dosing algorithms to predict warfarin maintenance dose in Caucasians and African Americans.

[PMID 19737746] Population differentiation as an indicator of recent positive selection in humans: an empirical evaluation.

[PMID 23238918] Genome-wide pathway analysis of a genome-wide association study on multiple sclerosis.

ClinVar
Risk	rs5896(T;T)
Alt	rs5896(T;T)
Reference	Rs5896(C;C)
Significance	Probable-non-pathogenic
Disease	not specified Hereditary factor II deficiency disease Thrombophilia
Variation	info
Gene	F2
CLNDBN	not specified Hereditary factor II deficiency disease Thrombophilia
Reversed	0
HGVS	NC_000011.9:g.46745003C>T
CLNSRC
CLNACC	RCV000243525.1, RCV000306522.1, RCV000396446.1,