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rs165774

From SNPedia

Orientationplus
Stabilizedplus
Make rs165774(A;A)
Make rs165774(A;G)
Make rs165774(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position19965038
GeneCOMT
is asnp
is mentioned by
dbSNPrs165774
ebirs165774
HLIrs165774
Exacrs165774
Varsomers165774
Maprs165774
PheGenIrs165774
hapmaprs165774
1000 genomesrs165774
hgdprs165774
ensemblrs165774
gopubmedrs165774
geneviewrs165774
scholarrs165774
googlers165774
pharmgkbrs165774
gwascentralrs165774
openSNPrs165774
23andMers165774
23andMe allrs165774
SNP Nexus

SNPshotrs165774
SNPdbers165774
MSV3drs165774
GWAS Ctlgrs165774
GMAF0.2287
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 20934310] HapMap tag-SNP analysis confirms a role for COMT in schizophrenia risk and reveals a novel association


[PMID 17442488] An association study between cathechol-O-methyltransferase gene and mental retardation in the Chinese Han population.


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


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


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


[PMID 21172166OA-icon.png] Pharmacogenetics of antidepressant response.


[PMID 24320736] Role of single nucleotide polymorphisms in estrogen-metabolizing enzymes and susceptibility to uterine leiomyoma in Han Chinese: A case-control study


[PMID 26207649] COMT gene locus: new functional variants


[PMID 26852906] Association of copy number polymorphisms at the promoter and translated region of COMT with Japanese patients with schizophrenia.


[PMID 27228319] A Tetra-Primer Amplification Refractory System Technique for the Cost-Effective and Novel Genotyping of Eight Single-Nucleotide Polymorphisms of the Catechol-O-Methyltransferase Gene.