Annotation Detail
Information
- Associated Genes
- CXCL12
- Associated Variants
-
CXCL12 c.*519G>A
(
ENST00000395793.7,
ENST00000374429.6 )
CXCL12 c.*519G>A ( ENST00000374429.6, ENST00000395793.7 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000609.7(CXCL12):c.*519G>A AND not provided
- ClinVar Allele ID
- 1280889
- ClinVar RefSeq Alternation Syntax
- NM_001277990.2:c.*79G>A
- ClinVar RefSeq Alternation Syntax
- NM_000609.7:c.*519G>A
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2018-11-12
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001715710
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs