Annotation Detail
Information
- Associated Genes
- PRAMEF1 PRAMEF2 CFAP107 AADACL3 AADACL4 HNRNPCL1 PRAMEF9 PRAMEF10 PRAMEF12 PRAMEF4 PRAMEF11 PRAMEF6 HNRNPCL2 PRAMEF7 PRAMEF25 PRAMEF26 HNRNPCL3 HNRNPCL4 PRAMEF27 LINC01784 LOC126805620 LOC126805621 LOC126805622
- Associated Variants
-
GRCh38/hg38 1p36.21(chr1:12666714-13181499)x3
GRCh38/hg38 1p36.21(chr1:12666714-13181499)x3 - Source Database
- ClinVar
- Description
- GRCh38/hg38 1p36.21(chr1:12666714-13181499)x3 AND See cases
- ClinVar Allele ID
- 156818
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2011-03-08
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000136288
- Observed Origin Sample
- not provided
Drugs