Annotation Detail
Information
- Associated Genes
- ARHGAP24
- Associated Variants
-
TP73 c.-20C>T
(
ENST00000378295.9,
ENST00000713572.1,
ENST00000354437.8,
ENST00000603362.6,
ENST00000604074.5,
ENST00000604479.6,
ENST00000713570.1 )
CDKN1A c.445+16C>G ( ENST00000244741.10, ENST00000373711.3, ENST00000405375.5, ENST00000448526.6, ENST00000615513.4 )
CDKN1A c.445+16C>T ( ENST00000244741.10, ENST00000373711.3, ENST00000405375.5, ENST00000448526.6, ENST00000615513.4 )
TP73 c.-20C>T ( ENST00000354437.8, ENST00000378295.9, ENST00000603362.6, ENST00000604074.5, ENST00000604479.6, ENST00000713570.1, ENST00000713572.1 )
CDKN1A c.445+16C>G ( ENST00000373711.3, ENST00000405375.5, ENST00000448526.6, ENST00000615513.4, ENST00000244741.10 )
CDKN1A c.445+16C>T ( ENST00000244741.10, ENST00000373711.3, ENST00000405375.5, ENST00000448526.6, ENST00000615513.4 ) - Associated Disease
- Esophageal Neoplasms
- Source Database
- DisGeNET
- Description
- p21 rs3176352 G>C and p73 rs1801173 C>T polymorphisms are associated with an increased risk of esophageal cancer in a Chinese population.
- Pubmed
- 24820515
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.00081432561624091
- Year of publication
- 2014
Drugs