Annotation Detail
Information
- Associated Genes
- CD36
- Associated Variants
-
Multiple alleles
(
ENST00000309881.11,
ENST00000435819.5,
ENST00000534394.5 )
Multiple alleles ( ENST00000309881.11, ENST00000435819.5, ENST00000534394.5 ) - Associated Disease
- type 2 diabetes mellitus
- Source Database
- ClinVar
- Description
- NM_001001547.3(CD36):c.-184+13244G>A AND Type 2 diabetes mellitus
- ClinVar Allele ID
- 480402
- ClinVar RefSeq Alternation Syntax
- NM_001371075.1:c.-184+13244G>A
- ClinVar RefSeq Alternation Syntax
- NM_001371080.1:c.-185+13244G>A
- ClinVar RefSeq Alternation Syntax
- NM_001371081.1:c.-666+13244G>A
- ClinVar RefSeq Alternation Syntax
- NM_001371074.1:c.-180+13244G>A
- ClinVar RefSeq Alternation Syntax
- NM_001001547.3:c.-184+13244G>A
- ClinVar RefSeq Alternation Syntax
- NM_001289911.2:c.-109+13244G>A
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2022-07-21
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002268206
- ClinVar Disease
- Type 2 diabetes mellitus
- Observed Origin Sample
- inherited
Drugs