Annotation Detail
Information
- Associated Genes
- IFNG
- Associated Variants
-
IFNG c.366+284G>A
(
ENST00000229135.4 )
IFNG c.366+284G>A ( ENST00000229135.4 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000619.3(IFNG):c.366+284G>A AND not provided
- ClinVar Allele ID
- 1250013
- ClinVar RefSeq Alternation Syntax
- NM_000619.3:c.366+284G>A
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2018-11-12
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001673626
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs