COMT c.-91-1375G>C

Variant ID: 22-19947347-G-C

NM_000754.4(COMT):c.-91-1375G>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


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: rs11912354
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



A common polymorphism of COMT was associated with symptomatic lumbar disc herniation based on a large sample with Chinese Han ancestry.

Scientific Reports
Liu, Hongliang H; Zhao, Hongmou H; Li, Zhong Z; Xue, Hanzhong H; Lu, Jun J; Ma, Wei W
Publication Date: 2018-08-29

Variant appearance in text: rs11912354
PubMed Link: 30158547
Variant Present in the following documents:
  • Main text
  • 41598_2018_Article_31240.pdf
View BVdb publication page