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rs4646316

From SNPedia

Orientationplus
Stabilizedplus
Make rs4646316(C;C)
Make rs4646316(C;T)
Make rs4646316(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position19964609
GeneCOMT
is asnp
is mentioned by
dbSNPrs4646316
ebirs4646316
HLIrs4646316
Exacrs4646316
Varsomers4646316
Maprs4646316
PheGenIrs4646316
hapmaprs4646316
1000 genomesrs4646316
hgdprs4646316
ensemblrs4646316
gopubmedrs4646316
geneviewrs4646316
scholarrs4646316
googlers4646316
pharmgkbrs4646316
gwascentralrs4646316
openSNPrs4646316
23andMers4646316
23andMe allrs4646316
SNP Nexus

SNPshotrs4646316
SNPdbers4646316
MSV3drs4646316
GWAS Ctlgrs4646316
GMAF0.2466
Max Magnitude
? (C;C) (C;T) (T;T) 28

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


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