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rs5896

From SNPedia

Orientationplus
Stabilizedplus
Make rs5896(C;C)
Make rs5896(C;T)
Make rs5896(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position46723453
GeneF2
is asnp
is mentioned by
dbSNPrs5896
ebirs5896
HLIrs5896
Exacrs5896
Varsomers5896
Maprs5896
PheGenIrs5896
hapmaprs5896
1000 genomesrs5896
hgdprs5896
ensemblrs5896
gopubmedrs5896
geneviewrs5896
scholarrs5896
googlers5896
pharmgkbrs5896
gwascentralrs5896
openSNPrs5896
23andMers5896
23andMe allrs5896
SNP Nexus

SNPshotrs5896
SNPdbers5896
MSV3drs5896
GWAS Ctlgrs5896
GMAF0.2452
Max Magnitude
? (C;C) (C;T) (T;T) 28

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


[PMID 16255080OA-icon.png] A haplotype map of the human genome.


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


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


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


[PMID 19737746OA-icon.png] 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.