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COMT c.-92+4358C>G
Variant ID: 22-19933778-C-G
NM_000754.4(
COMT
):c.-92+4358C>G
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:
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: rs174673
PubMed Link:
30158547
Variant Present in the following documents:
Main text
41598_2018_Article_31240.pdf
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: rs174673
PubMed Link:
20551675
Variant Present in the following documents:
Main text
View BVdb publication page