Annotation Detail
Information
- Associated Genes
- NOD2
- Associated Variants
-
NOD2 c.2798+265A>G
(
ENST00000300589.6,
ENST00000647318.2 )
NOD2 c.2798+265A>G ( ENST00000300589.6, ENST00000647318.2 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_001370466.1(NOD2):c.2717+265A>G AND not provided
- ClinVar Allele ID
- 1251679
- ClinVar RefSeq Alternation Syntax
- NM_001293557.2:c.2717+265A>G
- ClinVar RefSeq Alternation Syntax
- NM_022162.3:c.2798+265A>G
- ClinVar RefSeq Alternation Syntax
- NM_001370466.1:c.2717+265A>G
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2021-06-18
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001674351
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs