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rs3093200

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs3093200(A;A)
Make rs3093200(A;C)
ReferenceGRCh38 38.1/142
Chromosome19
Position15878779
GeneCYP4F2
is asnp
is mentioned by
dbSNPrs3093200
ebirs3093200
HLIrs3093200
Exacrs3093200
Varsomers3093200
Maprs3093200
PheGenIrs3093200
hapmaprs3093200
1000 genomesrs3093200
hgdprs3093200
ensemblrs3093200
gopubmedrs3093200
geneviewrs3093200
scholarrs3093200
googlers3093200
pharmgkbrs3093200
gwascentralrs3093200
openSNPrs3093200
23andMers3093200
23andMe allrs3093200
SNP Nexus

SNPshotrs3093200
SNPdbers3093200
MSV3drs3093200
GWAS Ctlgrs3093200
GMAF0.05969
Max Magnitude0
? (A;A) (A;C) (C;C) 28

[PMID 19097922] A haplotype of the CYP4F2 gene associated with myocardial infarction in Japanese men.


[PMID 18787519] A haplotype of the CYP4F2 gene is associated with cerebral infarction in Japanese men.


[PMID 18971550] Haplotype-based case-control study of the human CYP4F2 gene and essential hypertension in Japanese subjects.


[PMID 19957603] [Association on the haplotypes of CYP4F2 gene and myocardial infarction].


GET Evidence
CYP4F2-L519M
aa_change Leu519Met
aa_change_short L519M
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0791434
summary