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rs2292566

From SNPedia

Merged intors1131873
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs2292566(A;A)
Make rs2292566(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position225831952
GeneEPHX1
is asnp
is mentioned by
dbSNPrs2292566
ebirs2292566
HLIrs2292566
Exacrs2292566
Varsomers2292566
Maprs2292566
PheGenIrs2292566
hapmaprs2292566
1000 genomesrs2292566
hgdprs2292566
ensemblrs2292566
gopubmedrs2292566
geneviewrs2292566
scholarrs2292566
googlers2292566
pharmgkbrs2292566
gwascentralrs2292566
openSNPrs2292566
23andMers2292566
23andMe allrs2292566
SNP Nexus

SNPshotrs2292566
SNPdbers2292566
MSV3drs2292566
GWAS Ctlgrs2292566
StatusMerged into rs1131873
GMAF0.1781
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 19479063OA-icon.png] Phase I metabolic genes and risk of lung cancer: multiple polymorphisms and mRNA expression.


[PMID 21453055] Lack of association of EPHX1 genotypes and haplotypes with oral cancer in South Indians.


GET Evidence
rs2292566
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.142127
summary



[PMID 23061746] Impact of genetic factors (CYP2C9, VKORC1 and CYP4F2) on warfarin dose requirement in the Turkish population.