Annotation Detail
Information
- Associated Genes
- CLPTM1L
- Associated Variants
-
CLPTM1L c.1316-153G>A
(
ENST00000320895.10,
ENST00000507807.3,
ENST00000630539.1 )
CLPTM1L c.1316-153G>A ( ENST00000320895.10, ENST00000507807.3, ENST00000630539.1 ) - Associated Disease
- Malignant neoplasm of lung
- Source Database
- DisGeNET
- Description
- A common sequence variant, rs401681, located in an intronic region of CLPTM1L, has been reported to be associated with lung cancer risk based on genome-wide association study.
- Pubmed
- 24386361
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.142888331778182
- Year of publication
- 2013
Drugs