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rs8192488

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs8192488(C;T)
Make rs8192488(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position19963714
GeneCOMT, MIR4761
is asnp
is mentioned by
dbSNPrs8192488
ebirs8192488
HLIrs8192488
Exacrs8192488
Varsomers8192488
Maprs8192488
PheGenIrs8192488
hapmaprs8192488
1000 genomesrs8192488
hgdprs8192488
ensemblrs8192488
gopubmedrs8192488
geneviewrs8192488
scholarrs8192488
googlers8192488
pharmgkbrs8192488
gwascentralrs8192488
openSNPrs8192488
23andMers8192488
23andMe allrs8192488
SNP Nexus

SNPshotrs8192488
SNPdbers8192488
MSV3drs8192488
GWAS Ctlgrs8192488
GMAF0.02204
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 19365560OA-icon.png] Low enzymatic activity haplotypes of the human catechol-O-methyltransferase gene: enrichment for marker SNPs

[PMID 16816940] Direct molecular haplotyping of multiple polymorphisms within exon 4 of the human catechol-O-methyltransferase gene by liquid chromatography-electrospray ionization time-of-flight mass spectrometry.