Annotation Detail
Information
- Associated Genes
- RTEL1-TNFRSF6B
- Associated Variants
-
RTEL1 c.1037+140A>G, RTEL1-TNFRSF6B c.1121+140A>G
(
ENST00000318100.9,
ENST00000360203.11,
ENST00000370018.7,
ENST00000508582.7,
ENST00000492259.6 )
RTEL1 c.1349-771T>C, RTEL1-TNFRSF6B c.1433-771T>C ( ENST00000318100.9, ENST00000360203.11, ENST00000370018.7, ENST00000508582.7, ENST00000492259.6 )
RTEL1 c.1037+140A>G, RTEL1-TNFRSF6B c.1121+140A>G ( ENST00000318100.9, ENST00000360203.11, ENST00000370018.7, ENST00000508582.7, ENST00000492259.6 )
RTEL1 c.1349-771T>C, RTEL1-TNFRSF6B c.1433-771T>C ( ENST00000318100.9, ENST00000360203.11, ENST00000370018.7, ENST00000508582.7, ENST00000492259.6 ) - Associated Disease
- Glioma
- Source Database
- DisGeNET
- Description
- Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility.
- Pubmed
- 19578366
- Original source reporting the Gene Disease association
- GWASCAT
- DisGENET score for the Gene Disease association
- 0.12
- Year of publication
- 2009
Drugs