Annotation Detail
Information
- Associated Genes
- RNF166
- Associated Variants
-
CTU2 c.143+275C>T
(
ENST00000312060.9,
ENST00000567949.5,
ENST00000453996.7 )
CTU2 c.143+275C>T ( ENST00000312060.9, ENST00000453996.7, ENST00000567949.5 ) - Associated Disease
- Autism Spectrum Disorders
- Source Database
- DisGeNET
- Description
- A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?
- Pubmed
- 25534755
- Original source reporting the Gene Disease association
- GWASCAT
- DisGENET score for the Gene Disease association
- 0.12
- Year of publication
- 2014
Drugs