Annotation Detail
Information
- Associated Genes
- UCP1
- Associated Variants
-
NC_000004.12:g.140572807T>C
NC_000004.12:g.140572807T>C - Associated Disease
- UCP1 POLYMORPHISM
- Source Database
- ClinVar
- Description
- NC_000004.12:g.140572807T>C AND UCP1 POLYMORPHISM
- ClinVar Allele ID
- 32698
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2003-12-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000019227
- ClinVar Disease
- UCP1 POLYMORPHISM
- Observed Origin Sample
- germline
- Pubmed
- 8968850
- Pubmed
- 9398715
- Pubmed
- 10999801
- Pubmed
- 7951471
- Pubmed
- 14671150
Drugs