Annotation Detail
Information
- Associated Genes
- B3GLCT
- Associated Variants
-
B3GLCT c.271-1835T>C
(
ENST00000343307.5 )
B3GLCT c.271-1835T>C ( ENST00000343307.5 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_194318.4(B3GLCT):c.271-1835T>C AND not provided
- ClinVar Allele ID
- 171886
- ClinVar RefSeq Alternation Syntax
- NM_194318.4:c.271-1835T>C
- Clinical Significance Description
- not provided
- Clinical Significance Review Status
- no assertion provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000190310
- ClinVar Disease
- not provided
- Observed Origin Sample
- not provided
Drugs