Annotation Detail
Information
- Associated Genes
- MIR34B
- Associated Variants
-
BTG4 c.-27+341A>G
(
ENST00000689553.1,
ENST00000692032.1,
ENST00000356018.6,
ENST00000525791.5 )
NSRP1 c.20+302A>C ( ENST00000247026.10, ENST00000612959.4, ENST00000584423.5, ENST00000479218.6 )
NSRP1 c.20+302A>T ( ENST00000479218.6, ENST00000247026.10, ENST00000584423.5, ENST00000612959.4 )
BTG4 c.-27+341A>G ( ENST00000356018.6, ENST00000525791.5, ENST00000689553.1, ENST00000692032.1 )
NSRP1 c.20+302A>C ( ENST00000247026.10, ENST00000479218.6, ENST00000584423.5, ENST00000612959.4 )
NSRP1 c.20+302A>T ( ENST00000247026.10, ENST00000479218.6, ENST00000584423.5, ENST00000612959.4 ) - Associated Disease
- esophageal carcinoma
- Source Database
- DisGeNET
- Description
- Hsa-miR-34b/c rs4938723 T>C and hsa-miR-423 rs6505162 C>A polymorphisms are associated with the risk of esophageal cancer in a Chinese population.
- Pubmed
- 24260422
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.000271441872080303
- Year of publication
- 2013
Drugs