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rs165722

From SNPedia

Orientationplus
Stabilizedplus
Make rs165722(C;C)
Make rs165722(C;T)
Make rs165722(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position19961490
GeneCOMT
is asnp
is mentioned by
dbSNPrs165722
ebirs165722
HLIrs165722
Exacrs165722
Varsomers165722
Maprs165722
PheGenIrs165722
hapmaprs165722
1000 genomesrs165722
hgdprs165722
ensemblrs165722
gopubmedrs165722
geneviewrs165722
scholarrs165722
googlers165722
pharmgkbrs165722
gwascentralrs165722
openSNPrs165722
23andMers165722
23andMe allrs165722
SNP Nexus

SNPshotrs165722
SNPdbers165722
MSV3drs165722
GWAS Ctlgrs165722
GMAF0.4334
Max Magnitude

[PMID 21570824] Clinical and genetic factors associated with nausea and vomiting in cancer patients receiving opioids


[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 19693267OA-icon.png] Financial and psychological risk attitudes associated with two single nucleotide polymorphisms in the nicotine receptor (CHRNA4) gene.


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


[PMID 21423693OA-icon.png] Effect sizes in experimental pain produced by gender, genetic variants and sensitization procedures.