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rs3093105

From SNPedia

Orientationminus
Stabilizedminus
Make rs3093105(G;G)
Make rs3093105(G;T)
Make rs3093105(T;T)
ReferenceGRCh38 38.1/142
Chromosome19
Position15897578
GeneCYP4F2
is asnp
is mentioned by
dbSNPrs3093105
ebirs3093105
HLIrs3093105
Exacrs3093105
Varsomers3093105
Maprs3093105
PheGenIrs3093105
hapmaprs3093105
1000 genomesrs3093105
hgdprs3093105
ensemblrs3093105
gopubmedrs3093105
geneviewrs3093105
scholarrs3093105
googlers3093105
pharmgkbrs3093105
gwascentralrs3093105
openSNPrs3093105
23andMers3093105
23andMe allrs3093105
SNP Nexus

SNPshotrs3093105
SNPdbers3093105
MSV3drs3093105
GWAS Ctlgrs3093105
GMAF0.1566
Max Magnitude
? (G;G) (G;T) (T;T) 28

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


[PMID 18235092OA-icon.png] Association of a functional cytochrome P450 4F2 haplotype with urinary 20-HETE and hypertension.


[PMID 18250228OA-icon.png] CYP4F2 genetic variant alters required warfarin dose.


[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-W12G
aa_change Trp12Gly
aa_change_short W12G
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.191119
summary