Annotation Detail
Information
- Associated Genes
- APOE
- Associated Variants
-
APOE p.Arg165= (p.R165=)
(
ENST00000252486.9 )
APOE p.Arg165= (p.R165=) ( ENST00000252486.9 ) - Associated Disease
- APOE-related disorder
- Source Database
- ClinVar
- Description
- NM_000041.4(APOE):c.495G>T (p.Arg165=) AND APOE-related disorder
- ClinVar Allele ID
- 3206169
- ClinVar RefSeq Alternation Syntax
- NM_000041.4:c.495G>T
- ClinVar RefSeq Alternation Syntax
- NM_001302688.2:c.573G>T
- ClinVar RefSeq Alternation Syntax
- NM_001302690.2:c.495G>T
- ClinVar RefSeq Alternation Syntax
- NM_001302691.2:c.495G>T
- ClinVar RefSeq Alternation Syntax
- NM_001302689.2:c.495G>T
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2020-04-22
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003954895
- ClinVar Disease
- APOE-related disorder
- Observed Origin Sample
- germline
Drugs