Annotation Detail
Information
- Associated Genes
- PCDH11Y TGIF2LY
- Associated Variants
- GRCh37/hg19 Yp11.2(chrY:3069286-5670611)x2
- Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- GRCh37/hg19 Yp11.2(chrY:3069286-5670611)x2 AND not provided
- ClinVar Allele ID
- 556141
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2018-01-15
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000684432
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs