Annotation Detail
Information
- Associated Genes
- FGFR2
- Associated Variants
-
FGFR2 c.109+7033T>C
(
ENST00000360144.7,
ENST00000351936.11,
ENST00000369060.8,
ENST00000358487.10,
ENST00000369059.5,
ENST00000369056.5,
ENST00000359354.6,
ENST00000682550.1,
ENST00000611527.1,
ENST00000613048.4,
ENST00000457416.7,
ENST00000684153.1,
ENST00000356226.8,
ENST00000346997.6,
ENST00000369061.8,
ENST00000683211.1,
ENST00000357555.9,
ENST00000683035.1 )
ATE1 c.975+4331A>G ( ENST00000692329.1, ENST00000687089.1, ENST00000687583.1, ENST00000693411.1, ENST00000685289.1, ENST00000689057.1, ENST00000224652.12, ENST00000685072.1, ENST00000687458.1, ENST00000693276.1, ENST00000540606.7, ENST00000691765.1, ENST00000688057.1, ENST00000691573.1, ENST00000690355.1, ENST00000369040.9, ENST00000692278.1, ENST00000687144.1, ENST00000690773.1, ENST00000687935.1, ENST00000689834.1, ENST00000686907.1, ENST00000689393.1, ENST00000693486.1, ENST00000685007.1, ENST00000691830.1, ENST00000369043.8, ENST00000693655.1, ENST00000689571.1, ENST00000690415.1 )
FGFR2 c.109+7033T>C ( ENST00000346997.6, ENST00000351936.11, ENST00000356226.8, ENST00000357555.9, ENST00000358487.10, ENST00000359354.6, ENST00000360144.7, ENST00000369056.5, ENST00000369059.5, ENST00000369060.8, ENST00000369061.8, ENST00000457416.7, ENST00000611527.1, ENST00000613048.4, ENST00000682550.1, ENST00000683035.1, ENST00000683211.1, ENST00000684153.1 )
ATE1 c.975+4331A>G ( ENST00000224652.12, ENST00000369040.9, ENST00000369043.8, ENST00000540606.7, ENST00000685007.1, ENST00000685072.1, ENST00000685289.1, ENST00000686907.1, ENST00000687089.1, ENST00000687144.1, ENST00000687458.1, ENST00000687583.1, ENST00000687935.1, ENST00000688057.1, ENST00000689057.1, ENST00000689393.1, ENST00000689571.1, ENST00000689834.1, ENST00000690355.1, ENST00000690415.1, ENST00000690773.1, ENST00000691573.1, ENST00000691765.1, ENST00000691830.1, ENST00000692278.1, ENST00000692329.1, ENST00000693276.1, ENST00000693411.1, ENST00000693486.1, ENST00000693655.1 ) - Associated Disease
- Malignant neoplasm of breast
- Source Database
- DisGeNET
- Description
- A variant mapping to 10q26.13, approximately 300 kb telomeric to the established risk locus within the second intron of FGFR2, was also associated with breast cancer risk, although not at genome-wide statistical significance (rs10510102: OR = 1.12, 95% CI = 1.07 to 1.17, P = 1.58 × 10(-6)).
- Pubmed
- 21263130
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.229599312455182
- Year of publication
- 2011
Drugs