Annotation Detail
Information
- Associated Genes
- FGF9 GJA3 GJB2 ZMYM2 IFT88 ZMYM5 SAP18 GJB6 LATS2 CRYL1 IL17D XPO4 MRPL57 EEF1AKMT1 SKA3 MICU2 ZDHHC20 MIR4499 LINC00539 LINC00424 LOC101928764 LINC00367 LINC01046 LINC01072 LOC112163647 LOC121466728 LOC124849292 LOC126861703 LOC126861704 LOC126861705 LOC130009300 LOC130009301 LOC130009302 LOC130009303 LOC130009304 LOC130009305 LOC130009306 LOC130009307 LOC130009308 LOC130009309 LOC130009310 LOC130009311 LOC130009312 LOC130009313 LOC130009314 LOC130009315 LOC130009316 LOC130009317 LOC130009318 LOC130009319 LOC130009320 LOC130009321 LOC130009322 LOC130009323 LOC130009324 LOC130009325 LOC130009326 LOC130009327 LOC130009328 LOC130009329 LOC130009330 LOC130009331 LOC130009332 LOC130009333 LOC130009334 LOC130009335 LOC130009336 LOC130009337 LOC130009338 LOC130009339 LOC130009340 LOC130009341 LOC130009342 LOC130009343 LOC130009344 LOC130009345 LOC130009346 LOC130009347 LOC130009348 LOC130009349 LOC130009350 LOC130009351 LOC130009352 LOC130009353 LOC130009354 LOC132090175
- Associated Variants
-
GRCh38/hg38 13q12.11(chr13:19837395-21967789)x1
GRCh38/hg38 13q12.11(chr13:19837395-21967789)x1 - Source Database
- ClinVar
- Description
- GRCh38/hg38 13q12.11(chr13:19837395-21967789)x1 AND See cases
- ClinVar Allele ID
- 157748
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2010-12-22
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000137093
- Observed Origin Sample
- not provided
Drugs