Annotation Detail
Information
- Associated Genes
- POLG POLGARF
- Associated Variants
-
POLG p.Gly11Asp (p.G11D), POLGARF p.Arg29= (p.R29=)
(
ENST00000706918.1,
ENST00000636937.2,
ENST00000268124.11,
ENST00000442287.6 )
POLG p.Gly11Asp (p.G11D), POLGARF p.Arg29= (p.R29=) ( ENST00000268124.11, ENST00000442287.6, ENST00000636937.2, ENST00000706918.1 ) - Associated Disease
- Inborn genetic diseases
- Source Database
- ClinVar
- Description
- NM_002693.3(POLG):c.32G>A (p.Gly11Asp) AND Inborn genetic diseases
- ClinVar Allele ID
- 192343
- ClinVar RefSeq Alternation Syntax
- NM_002693.3:c.32G>A
- ClinVar RefSeq Alternation Syntax
- NM_001126131.2:c.32G>A
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2022-05-31
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002453618
- ClinVar Disease
- Inborn genetic diseases
- Observed Origin Sample
- germline
Drugs