Annotation Detail
Information
- Associated Genes
- ACAT1 ATM CASP1 CASP4 CASP5 CRYAB DDX10 DLAT DRD2 FDX1 GRIA4 GUCY1A2 HSPB2 HTR3A IL18 NCAM1 NNMT NPAT POU2AF1 PPP2R1B PTS RDX SDHD SLN ZBTB16 CUL5 ZPR1 HTR3B ZW10 RBM7 EXPH5 SIK2 CADM1 REXO2 TIMM8B C11orf71 SLC35F2 RAB39A BTG4 NXPE4 TTC12 NKAPD1 ELMOD1 TEX12 ARHGAP20 USP28 CARD18 AASDHPPT CFAP68 ALG9 TMPRSS5 BCO2 MSANTD4 BUD13 DIXDC1 ZC3H12C ALKBH8 FDXACB1 C11orf52 CARD16 APOA5 POU2AF3 PIH1D2 NXPE1 NXPE2 KBTBD3 CWF19L2 POGLUT3 LAYN C11orf65 ANKK1 POU2AF2 PLET1 C11orf87 HOATZ MIR34B MIR34C CARD17P CLDN25 MIR34BHG LOC100132686 CASP12
- Associated Variants
- GRCh37/hg19 11q22.3-23.3(chr11:104101411-116680918)x1
- Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- GRCh37/hg19 11q22.3-23.3(chr11:104101411-116680918)x1 AND not provided
- ClinVar Allele ID
- 675642
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2017-09-26
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000848741
- ClinVar Disease
- not provided
- Observed Origin Sample
- unknown
Drugs