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