Annotation Detail
Information
- Associated Genes
- APLP1 CAPNS1 TBCB COX7A1 NPHS1 POLR2I TYROBP ZNF146 HCST CLIP3 LRFN3 KIRREL2 NFKBID ALKBH6 ZNF565 SYNE4 THAP8 WDR62 SDHAF1 OVOL3
- Associated Variants
- GRCh37/hg19 19q13.12(chr19:36312941-36751702)x3
- Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- GRCh37/hg19 19q13.12(chr19:36312941-36751702)x3 AND not provided
- ClinVar Allele ID
- 2845926
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2023-01-04
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003485199
- ClinVar Disease
- not provided
- Observed Origin Sample
- unknown
Drugs