Annotation Detail
Information
- Associated Genes
- G6PD
- Associated Variants
-
NM_001360016.2(G6PD):c.1365-13C>T AND not provided
G6PD c.1365-13C>T ( ENST00000369620.6, ENST00000393562.10, ENST00000393564.7, ENST00000439227.6, ENST00000696420.1, ENST00000696421.1, ENST00000696429.1, ENST00000696430.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_001360016.2(G6PD):c.1365-13C>T AND not provided
- ClinVar Allele ID
- 982298
- ClinVar RefSeq Alternation Syntax
- NM_001360016.2:c.1365-13C>T
- ClinVar RefSeq Alternation Syntax
- NM_001042351.3:c.1365-13C>T
- ClinVar RefSeq Alternation Syntax
- NM_000402.4:c.1455-13C>T
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2022-02-18
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001810579
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs