Annotation Detail
Information
- Associated Genes
- MC4R
- Associated Variants
-
MC4R p.Asp37Val (p.D37V)
(
ENST00000299766.5 )
MC4R p.Asp37Val (p.D37V) ( ENST00000299766.5 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_005912.2(MC4R):c.110A>T (p.Asp37Val) AND not provided
- ClinVar Allele ID
- 29358
- ClinVar RefSeq Alternation Syntax
- NM_005912.3:c.110A>T
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2023-12-16
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001699179
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs