Annotation Detail
Information
- Associated Genes
- OGG1
- Associated Variants
-
OGG1 c.948+273C>G
(
ENST00000302003.11,
ENST00000302008.12,
ENST00000302036.12,
ENST00000339511.9,
ENST00000344629.12,
ENST00000352937.6,
ENST00000383826.9,
ENST00000449570.6,
ENST00000707074.1 )
OGG1 c.948+273C>G ( ENST00000302003.11, ENST00000302008.12, ENST00000302036.12, ENST00000339511.9, ENST00000344629.12, ENST00000352937.6, ENST00000383826.9, ENST00000449570.6, ENST00000707074.1 ) - Associated Disease
- Hearing Loss, Mixed Conductive-Sensorineural
- Source Database
- DisGeNET
- Description
- A functional Ser326Cys polymorphism in hOGG1 is associated with noise-induced hearing loss in a Chinese population.
- Pubmed
- 24599382
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.000271441872080303
- Year of publication
- 2014
Drugs