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rs2020917

From SNPedia

Orientationplus
Stabilizedplus
Make rs2020917(C;C)
Make rs2020917(C;T)
Make rs2020917(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position19941361
GeneCOMT, TXNRD2
is asnp
is mentioned by
dbSNPrs2020917
ebirs2020917
HLIrs2020917
Exacrs2020917
Varsomers2020917
Maprs2020917
PheGenIrs2020917
hapmaprs2020917
1000 genomesrs2020917
hgdprs2020917
ensemblrs2020917
gopubmedrs2020917
geneviewrs2020917
scholarrs2020917
googlers2020917
pharmgkbrs2020917
gwascentralrs2020917
openSNPrs2020917
23andMers2020917
23andMe allrs2020917
SNP Nexus

SNPshotrs2020917
SNPdbers2020917
MSV3drs2020917
GWAS Ctlgrs2020917
GMAF0.2282
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 16848906OA-icon.png] Genetic polymorphisms in monoamine neurotransmitter systems show only weak association with acute post-surgical pain in humans.


[PMID 18436194OA-icon.png] Catechol-O-methyltransferase contributes to genetic susceptibility shared among anxiety spectrum phenotypes.


[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.


GET Evidence
rs2020917
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.185484
summary



[PMID 22705295] Association of MB-COMT polymorphisms with schizophrenia-susceptibility and symptom severity in an African cohort.


[PMID 23351565] Potential role of membrane-bound COMT gene polymorphisms in female depression vulnerability.