Annotation Detail
Information
- Associated Genes
- CFHR4
- Associated Variants
-
CFHR4 c.1541-159T>G
(
ENST00000367416.6,
ENST00000608469.6,
ENST00000251424.8 )
CFHR4 c.1541-159T>G ( ENST00000251424.8, ENST00000367416.6, ENST00000608469.6 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_001201550.3(CFHR4):c.1541-159T>G AND not provided
- ClinVar Allele ID
- 1257072
- ClinVar RefSeq Alternation Syntax
- NM_001201550.3:c.1541-159T>G
- ClinVar RefSeq Alternation Syntax
- NM_006684.5:c.800-159T>G
- ClinVar RefSeq Alternation Syntax
- NM_001201551.2:c.1538-159T>G
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2018-11-10
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001670718
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs