Annotation Detail
Information
- Associated Genes
- LGALS3BP TIMP2 DNAH17 CYTH1 USP36 ENGASE C1QTNF1 CANT1 RBFOX3 C1QTNF1-AS1 CEP295NL DNAH17-AS1 SCAT1 LOC112533675 LOC112533676 LOC116276482 LOC121627815 LOC121852953 LOC125316808 LOC126862653 LOC126862654 LOC126862655 LOC126862656 LOC126862657 LOC126862658 LOC129390942 LOC129390943 LOC129390944 LOC130061846 LOC130061847 LOC130061848 LOC130061849 LOC130061850 LOC130061851 LOC130061852 LOC130061853 LOC130061854 LOC130061855 LOC130061856 LOC130061857 LOC130061858 LOC130061859 LOC130061860 LOC130061861 LOC130061862 LOC130061863 LOC130061864 LOC130061865 LOC130061866 LOC130061867 LOC130061868 LOC130061869 LOC130061870 LOC130061871 LOC130061872 LOC132090480 LOC132090481
- Associated Variants
-
GRCh38/hg38 17q25.3(chr17:78484862-79436025)x4
GRCh38/hg38 17q25.3(chr17:78484862-79436025)x4 - Source Database
- ClinVar
- Description
- GRCh38/hg38 17q25.3(chr17:78484862-79436025)x4 AND See cases
- ClinVar Allele ID
- 163125
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2013-05-29
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000141790
- Observed Origin Sample
- not provided
Drugs