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rs740602

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs740602(A;A)
Make rs740602(A;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position19962745
GeneCOMT, MIR4761
is asnp
is mentioned by
dbSNPrs740602
ebirs740602
HLIrs740602
Exacrs740602
Varsomers740602
Maprs740602
PheGenIrs740602
hapmaprs740602
1000 genomesrs740602
hgdprs740602
ensemblrs740602
gopubmedrs740602
geneviewrs740602
scholarrs740602
googlers740602
pharmgkbrs740602
gwascentralrs740602
openSNPrs740602
23andMers740602
23andMe allrs740602
SNP Nexus

SNPshotrs740602
SNPdbers740602
MSV3drs740602
GWAS Ctlgrs740602
GMAF0.05051
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.