Annotation Detail
Information
- Associated Genes
- APBB1 CCKBR TPP1 CNGA4 HPX ILK SMPD1 TAF10 DCHS1 TRIM3 RRP8 ARFIP2 TIMM10B MRPL17 FHIP1B CAVIN3 OR52W1 OR56A4 OR56A1 DNHD1 C11orf42 OR56B4 OR52B2 OR52L1 OR52E4 OR56A3 OR56A5
- Associated Variants
- GRCh37/hg19 11p15.4(chr11:5896551-6719852)x3
- Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- GRCh37/hg19 11p15.4(chr11:5896551-6719852)x3 AND not provided
- ClinVar Allele ID
- 676872
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2018-04-05
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000849971
- ClinVar Disease
- not provided
- Observed Origin Sample
- unknown
Drugs