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rs1558139

From SNPedia

Orientationplus
Stabilizedplus
Make rs1558139(A;A)
Make rs1558139(A;G)
Make rs1558139(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position15886754
GeneCYP4F2
is asnp
is mentioned by
dbSNPrs1558139
ebirs1558139
HLIrs1558139
Exacrs1558139
Varsomers1558139
Maprs1558139
PheGenIrs1558139
hapmaprs1558139
1000 genomesrs1558139
hgdprs1558139
ensemblrs1558139
gopubmedrs1558139
geneviewrs1558139
scholarrs1558139
googlers1558139
pharmgkbrs1558139
gwascentralrs1558139
openSNPrs1558139
23andMers1558139
23andMe allrs1558139
SNP Nexus

SNPshotrs1558139
SNPdbers1558139
MSV3drs1558139
GWAS Ctlgrs1558139
GMAF0.4293
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 18971550] rs1558139 might be a genetic marker for EH and the T-T-G haplotype might be a protective genetic marker for essential hypertension in Japanese men.


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


[PMID 17903306OA-icon.png] Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study.


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


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