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rs5993882

From SNPedia

Orientationplus
Stabilizedplus
Make rs5993882(G;G)
Make rs5993882(G;T)
Make rs5993882(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position19950010
GeneCOMT
is asnp
is mentioned by
dbSNPrs5993882
ebirs5993882
HLIrs5993882
Exacrs5993882
Varsomers5993882
Maprs5993882
PheGenIrs5993882
hapmaprs5993882
1000 genomesrs5993882
hgdprs5993882
ensemblrs5993882
gopubmedrs5993882
geneviewrs5993882
scholarrs5993882
googlers5993882
pharmgkbrs5993882
gwascentralrs5993882
openSNPrs5993882
23andMers5993882
23andMe allrs5993882
SNP Nexus

SNPshotrs5993882
SNPdbers5993882
MSV3drs5993882
GWAS Ctlgrs5993882
GMAF0.2433
Max Magnitude
? (G;G) (G;T) (T;T) 28
This is one of the SNPs reported by NutraHacker.


[PMID 16848906OA-icon.png] Genetic polymorphisms in monoamine neurotransmitter systems show only weak association with acute post-surgical pain in humans.


[PMID 18574484OA-icon.png] The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase.


[PMID 19772600OA-icon.png] A comparison of classification methods for predicting Chronic Fatigue Syndrome based on genetic data.


[PMID 22337325] The effect of catechol-O-methyltransferase polymorphisms on pain is modified by depressive symptoms.