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rs4646312

From SNPedia

Orientationplus
Stabilizedplus
Make rs4646312(C;C)
Make rs4646312(C;T)
Make rs4646312(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position19960814
GeneCOMT
is asnp
is mentioned by
dbSNPrs4646312
ebirs4646312
HLIrs4646312
Exacrs4646312
Varsomers4646312
Maprs4646312
PheGenIrs4646312
hapmaprs4646312
1000 genomesrs4646312
hgdprs4646312
ensemblrs4646312
gopubmedrs4646312
geneviewrs4646312
scholarrs4646312
googlers4646312
pharmgkbrs4646312
gwascentralrs4646312
openSNPrs4646312
23andMers4646312
23andMe allrs4646312
SNP Nexus

SNPshotrs4646312
SNPdbers4646312
MSV3drs4646312
GWAS Ctlgrs4646312
GMAF0.3136
Max Magnitude
? (C;C) (C;T) (T;T) 28
This is one of the SNPs reported by NutraHacker.


[PMID 16848906OA-icon.png] Genetic polymorphisms in monoamine neurotransmitter systems show only weak association with acute post-surgical pain in humans.


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


[PMID 19015200OA-icon.png] Polymorphisms in estrogen- and androgen-metabolizing genes and the risk of gastric cancer.


[PMID 19693267OA-icon.png] Financial and psychological risk attitudes associated with two single nucleotide polymorphisms in the nicotine receptor (CHRNA4) gene.


[PMID 19772600OA-icon.png] A comparison of classification methods for predicting Chronic Fatigue Syndrome based on genetic data.


[PMID 21423693OA-icon.png] Effect sizes in experimental pain produced by gender, genetic variants and sensitization procedures.


[PMID 25927430] Association of DRD3, COMT, and SLC6A4 Gene Polymorphisms with Type 2 Diabetes in Southern Chinese: A Hospital-Based Case-Control Study