Annotation Detail
Information
- Associated Genes
- MAOA
- Associated Variants
-
MAOA p.Arg297= (p.R297=)
(
ENST00000338702.4,
ENST00000542639.6,
ENST00000686683.1,
ENST00000688006.1,
ENST00000689087.1,
ENST00000693128.1 )
MAOA p.Arg297= (p.R297=) ( ENST00000338702.4, ENST00000542639.6, ENST00000686683.1, ENST00000688006.1, ENST00000689087.1, ENST00000693128.1 ) - Associated Disease
- Inborn genetic diseases
- Source Database
- ClinVar
- Description
- NM_000240.4(MAOA):c.891G>T (p.Arg297=) AND Inborn genetic diseases
- ClinVar Allele ID
- 98571
- ClinVar RefSeq Alternation Syntax
- NM_001270458.2:c.492G>T
- ClinVar RefSeq Alternation Syntax
- NM_000240.4:c.891G>T
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2015-06-22
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002311551
- ClinVar Disease
- Inborn genetic diseases
- Observed Origin Sample
- germline
Drugs