Annotation Detail
Information
- Associated Genes
- PGK1
- Associated Variants
-
PGK1 c.756+5G>A
(
ENST00000373316.5,
ENST00000644362.1 )
PGK1 c.756+5G>A ( ENST00000373316.5, ENST00000644362.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000291.4(PGK1):c.756+5G>A AND not provided
- ClinVar Allele ID
- 24994
- ClinVar RefSeq Alternation Syntax
- NM_000291.4:c.756+5G>A
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2023-03-14
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003555996
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs