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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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