Annotation Detail
Information
- Associated Genes
- INSR
- Associated Variants
-
INSR c.1861+56T>C
(
ENST00000302850.10,
ENST00000341500.9 )
INSR c.1861+56T>C ( ENST00000302850.10, ENST00000341500.9 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000208.4(INSR):c.1861+56T>C AND not provided
- ClinVar Allele ID
- 1243550
- ClinVar RefSeq Alternation Syntax
- NM_001079817.3:c.1861+56T>C
- ClinVar RefSeq Alternation Syntax
- NM_000208.4:c.1861+56T>C
- 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/RCV001663169
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs