RUNX2 c.58+43330T>C

Variant ID: 6-45339851-T-C

NM_001024630.3(RUNX2):c.58+43330T>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genetics of Degenerative Cervical Myelopathy: A Systematic Review and Meta-Analysis of Candidate Gene Studies.

Journal Of Clinical Medicine
Pope, Daniel H DH; Davies, Benjamin M BM; Mowforth, Oliver D OD; Bowden, A Ramsay AR; Kotter, Mark R N MRN
Publication Date: 2020-01-20

Variant appearance in text: rs16873379
PubMed Link: 31968564
Variant Present in the following documents:
  • Main text
  • jcm-09-00282.pdf
View BVdb publication page



Role of Runx2 polymorphisms in risk and prognosis of ossification of posterior longitudinal ligament.

Journal Of Clinical Laboratory Analysis
Chang, Feng F; Li, Lijun L; Gao, Gang G; Ding, Shengqiang S; Yang, Jincai J; Zhang, Ting T; Zuo, Genle G
Publication Date: 2017-07

Variant appearance in text: rs16873379
PubMed Link: 27704615
Variant Present in the following documents:
  • Main text
View BVdb publication page