COMT c.98T>C ;(p.L33P)

Variant ID: 22-19950147-T-C

NM_000754.3(COMT):c.98T>C;(p.L33P)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genetic Markers for Thrombophilia and Cardiovascular Disease Associated with Multiple Sclerosis.

Biomedicines
Hadjiagapiou, Maria S MS; Krashias, George G; Deeba, Elie E; Kallis, George G; Papaloizou, Andri A; Costeas, Paul P; Christodoulou, Christina C; Pantzaris, Marios M; Lambrianides, Anastasia A
Publication Date: 2022-10-21

Variant appearance in text: COMT: Leu33Pro
PubMed Link: 36289926
Variant Present in the following documents:
  • biomedicines-10-02665.pdf
View BVdb publication page



Are we creating a new phenotype? Physiological barriers and ethical considerations in the treatment of hereditary transthyretin-amyloidosis.

Neurological Research And Practice
Dohrn, Maike F MF; Medina, Jessica J; Olaciregui Dague, Karmele R KR; Hund, Ernst E
Publication Date: 2021-11-01

Variant appearance in text: COMT: Leu33Pro
PubMed Link: 34719408
Variant Present in the following documents:
  • Main text
  • 42466_2021_Article_155.pdf
View BVdb publication page