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rs933271

From SNPedia

Orientationplus
Stabilizedplus
Make rs933271(C;C)
Make rs933271(C;T)
Make rs933271(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position19943884
GeneCOMT
is asnp
is mentioned by
dbSNPrs933271
ebirs933271
HLIrs933271
Exacrs933271
Varsomers933271
Maprs933271
PheGenIrs933271
hapmaprs933271
1000 genomesrs933271
hgdprs933271
ensemblrs933271
gopubmedrs933271
geneviewrs933271
scholarrs933271
googlers933271
pharmgkbrs933271
gwascentralrs933271
openSNPrs933271
23andMers933271
23andMe allrs933271
SNP Nexus

SNPshotrs933271
SNPdbers933271
MSV3drs933271
GWAS Ctlgrs933271
GMAF0.3866
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 23269216] Association between the COMT gene and rumination in a Hungarian sample


[PMID 16395295] Significant association of catechol-O-methyltransferase (COMT) haplotypes with nicotine dependence in male and female smokers of two ethnic populations.


[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 19673036OA-icon.png] Association of tagging single nucleotide polymorphisms on 8 candidate genes in dopaminergic pathway with schizophrenia in Croatian population.


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


[PMID 21656904OA-icon.png] Association between polymorphisms in catechol-O-methyltransferase (COMT) and cocaine-induced paranoia in European-American and African-American populations.


[PMID 23008195] Genetic variants in the catechol-o-methyltransferase gene are associated with impulsivity and executive function: relevance for major depression.