Annotation Detail
Information
- Associated Genes
- FASLG
- Associated Variants
-
NC_000001.11:g.172658358C>T
NC_000001.11:g.172658358C>T - Associated Disease
- Autoimmune lymphoproliferative syndrome type 1
- Source Database
- ClinVar
- Description
- NC_000001.11:g.172658358C>T AND Autoimmune lymphoproliferative syndrome type 1
- ClinVar Allele ID
- 1153359
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2024-01-19
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001511738
- ClinVar Disease
- Autoimmune lymphoproliferative syndrome type 1
- Observed Origin Sample
- germline
Drugs