Annotation Detail
Information
- Associated Genes
- CRP
- Associated Variants
-
CRP c.*1082G>A
(
ENST00000368112.5,
ENST00000437342.1,
ENST00000255030.9 )
CRP c.*1082G>A ( ENST00000255030.9, ENST00000368112.5, ENST00000437342.1 ) - Associated Disease
- Inflammation
- Source Database
- ClinVar
- Description
- NM_000567.3(CRP):c.*1082G>A AND Inflammation
- ClinVar Allele ID
- 1685435
- ClinVar RefSeq Alternation Syntax
- NM_000567.3:c.*1082G>A
- ClinVar RefSeq Alternation Syntax
- NM_001382703.1:c.*1082G>A
- ClinVar RefSeq Alternation Syntax
- NM_001329058.2:c.*148G>A
- ClinVar RefSeq Alternation Syntax
- NM_001329057.2:c.*374G>A
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002259422
- ClinVar Disease
- Inflammation
- Observed Origin Sample
- unknown
Drugs