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rs769224

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0
Make rs769224(A;A)
Make rs769224(A;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position19964281
GeneCOMT, MIR4761
is asnp
is mentioned by
dbSNPrs769224
ebirs769224
HLIrs769224
Exacrs769224
Varsomers769224
Maprs769224
PheGenIrs769224
hapmaprs769224
1000 genomesrs769224
hgdprs769224
ensemblrs769224
gopubmedrs769224
geneviewrs769224
scholarrs769224
googlers769224
pharmgkbrs769224
gwascentralrs769224
openSNPrs769224
23andMers769224
23andMe allrs769224
SNP Nexus

SNPshotrs769224
SNPdbers769224
MSV3drs769224
GWAS Ctlgrs769224
GMAF0.04729
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 19365560OA-icon.png] Low enzymatic activity haplotypes of the human catechol-O-methyltransferase gene: enrichment for marker SNPs

[PMID 18574484OA-icon.png] The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase.

[PMID 21680027] Influence and interaction of genetic polymorphisms in catecholamine neurotransmitter systems and early life stress on antidepressant drug response.


[PMID 24174958OA-icon.png] Mercury Promotes Catecholamines Which Potentiate Mercurial Autoimmunity and Vasodilation: Implications for Inositol 1,4,5-Triphosphate 3-Kinase C Susceptibility in Kawasaki Syndrome