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rs2239393

From SNPedia

Orientationplus
Stabilizedplus
Make rs2239393(A;A)
Make rs2239393(A;G)
Make rs2239393(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position19962905
GeneCOMT, MIR4761
is asnp
is mentioned by
dbSNPrs2239393
ebirs2239393
HLIrs2239393
Exacrs2239393
Varsomers2239393
Maprs2239393
PheGenIrs2239393
hapmaprs2239393
1000 genomesrs2239393
hgdprs2239393
ensemblrs2239393
gopubmedrs2239393
geneviewrs2239393
scholarrs2239393
googlers2239393
pharmgkbrs2239393
gwascentralrs2239393
openSNPrs2239393
23andMers2239393
23andMe allrs2239393
SNP Nexus

SNPshotrs2239393
SNPdbers2239393
MSV3drs2239393
GWAS Ctlgrs2239393
GMAF0.3811
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 21206424OA-icon.png] Novel Polymorphisms Associated With Tacrolimus Trough Concentrations: Results From a Multicenter Kidney Transplant Consortium


[PMID 18937309OA-icon.png] Sexually dimorphic effects of four genes (COMT, SLC6A2, MAOA, SLC6A4) in genetic associations of ADHD: a preliminary study.


[PMID 19094200OA-icon.png] Genetic variation in the catechol-O-methyltransferase (COMT) gene and morphine requirements in cancer patients with pain.