Annotation Detail
Information
- Associated Genes
- CDKN2B
- Associated Variants
-
RTEL1 c.1037+140A>G, RTEL1-TNFRSF6B c.1121+140A>G
(
ENST00000318100.9,
ENST00000360203.11,
ENST00000370018.7,
ENST00000508582.7,
ENST00000492259.6 )
rs4295627
rs4977756
RTEL1 c.1037+140A>G, RTEL1-TNFRSF6B c.1121+140A>G ( ENST00000318100.9, ENST00000360203.11, ENST00000370018.7, ENST00000508582.7, ENST00000492259.6 )
rs4295627
rs4977756 - Associated Disease
- Glioma
- Source Database
- DisGeNET
- Description
- Three of the gene variants (rs4295627, a variant of CCDC26; rs4977756, a variant of CDKN2A and CDKN2B; and rs6010620, a variant of RTEL1) were statistically significantly associated with glioma risk in the present population.
- Pubmed
- 21920947
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.135982732844335
- Year of publication
- 2011
Drugs