Annotation Detail
Information
- Associated Genes
- SOD2
- Associated Variants
-
SOD2 p.Val16Ala (p.V16A)
(
ENST00000337404.8,
ENST00000367054.6,
ENST00000367055.8,
ENST00000444946.6,
ENST00000452684.2,
ENST00000538183.7,
ENST00000546087.5 )
SOD2 p.Val16Ala (p.V16A) ( ENST00000337404.8, ENST00000367054.6, ENST00000367055.8, ENST00000444946.6, ENST00000452684.2, ENST00000538183.7, ENST00000546087.5 ) - Associated Disease
- Hearing Loss, Mixed Conductive-Sensorineural
- Source Database
- DisGeNET
- Description
- The C allele of SOD2 (rs4880) was more frequent in Ménière's disease cases with a hearing level over 50 dB compared with cases with a hearing level below 50 dB, suggesting that this polymorphism is associated with progression of a hearing loss in Ménière's disease.
- Pubmed
- 22877234
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.00081432561624091
- Year of publication
- 2012
Drugs