Annotation Detail
Information
- Associated Genes
- EGFR
- Associated Variants
-
EGFR c.89-50630A>G
(
ENST00000275493.7,
ENST00000342916.7,
ENST00000344576.7,
ENST00000420316.6,
ENST00000455089.5 )
EGFR c.89-50630A>T ( ENST00000275493.7, ENST00000342916.7, ENST00000344576.7, ENST00000420316.6, ENST00000455089.5 )
EGFR c.89-50630A>G ( ENST00000275493.7, ENST00000342916.7, ENST00000344576.7, ENST00000420316.6, ENST00000455089.5 )
EGFR c.89-50630A>T ( ENST00000275493.7, ENST00000342916.7, ENST00000344576.7, ENST00000420316.6, ENST00000455089.5 ) - Associated Disease
- Glioma
- Source Database
- DisGeNET
- Description
- [Chromosome 7p11.2 (EGFR) variation influences glioma risk.]
- Pubmed
- 21531791
- Original source reporting the Gene Disease association
- GAD
- DisGENET score for the Gene Disease association
- 0.222572316166083
- Year of publication
- 2011
Drugs