COMT c.-91-780C>A

Variant ID: 22-19947942-C-A

NM_000754.4(COMT):c.-91-780C>A

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Grading Evolution and Contemporary Prognostic Biomarkers of Clinically Significant Prostate Cancer.

Cancers
Sopyllo, Konrad K; Erickson, Andrew M AM; Mirtti, Tuomas T
Publication Date: 2021-02-05

Variant appearance in text: rs16982844
PubMed Link: 33562508
Variant Present in the following documents:
  • Main text
  • cancers-13-00628.pdf
View BVdb publication page



Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs16982844
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Localizing putative markers in genetic association studies by incorporating linkage disequilibrium into bayesian hierarchical models.

Human Heredity
Fridley, Brooke L BL; Jenkins, Gregory D GD
Publication Date: 2010

Variant appearance in text: rs16982844
PubMed Link: 20551675
Variant Present in the following documents:
  • Main text
View BVdb publication page